Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80108705_80108706insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA , CM000679.2:g.80108705_80108706insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	GRCh38
NC_000017.10:g.78082504_78082505insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA , CM000679.1:g.78082504_78082505insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	GRCh37
NC_000017.9:g.75697099_75697100insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NCBI36
NG_009822.1:g.12150_12151insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA , LRG_673:g.12150_12151insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	ENSP00000460543.2:p.Trp402GlufsTer?
ENST00000572080.2:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	ENSP00000459972.2:p.Trp402GlufsTer?
ENST00000577106.6:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	ENSP00000458306.2:p.Trp402GlufsTer?
ENST00000302262.8:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA MANE Select	ENSP00000305692.3:p.Trp402GlufsTer?
ENST00000302262.7:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	ENSP00000305692.3:p.Trp402GlufsTer?
ENST00000390015.7:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	ENSP00000374665.3:p.Trp402GlufsTer?
NM_000152.3:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA , LRG_673t1:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_000143.2:p.Trp402GlufsTer?
NM_001079803.1:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_001073271.1:p.Trp402GlufsTer?
NM_001079804.1:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_001073272.1:p.Trp402GlufsTer?
XM_005257193.1:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	XP_005257250.1:p.Trp402GlufsTer?
XM_005257194.3:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	XP_005257251.1:p.Trp402GlufsTer?
NM_000152.4:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_000143.2:p.Trp402GlufsTer?
NM_001079803.2:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_001073271.1:p.Trp402GlufsTer?
NM_001079804.2:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_001073272.1:p.Trp402GlufsTer?
XM_005257193.2:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	XP_005257250.1:p.Trp402GlufsTer?
XM_005257194.4:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	XP_005257251.1:p.Trp402GlufsTer?
NM_000152.5:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA MANE Select	NP_000143.2:p.Trp402GlufsTer?
NM_001079803.3:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_001073271.1:p.Trp402GlufsTer?
NM_001079804.3:c.1203_1204insGAACGACACGGGACCGTCTGCTGGGGCCTGAGGAGACGGTCCCGTGTTGTGGCTGCAGGACGTCCAA	NP_001073272.1:p.Trp402GlufsTer?