Allele Registry

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Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80118208dup , CM000679.2:g.80118208dup	GRCh38
NC_000017.10:g.78092007dup , CM000679.1:g.78092007dup	GRCh37
NC_000017.9:g.75706602dup	NCBI36
NG_009822.1:g.21653dup , LRG_673:g.21653dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.2497dup	ENSP00000460543.2:p.Thr833AsnfsTer?
ENST00000572080.2:c.*635dup	ENSP00000459972.2:n.*635dup
ENST00000577106.6:c.2497dup	ENSP00000458306.2:p.Thr833AsnfsTer?
ENST00000302262.8:c.2497dup MANE Select	ENSP00000305692.3:p.Thr833AsnfsTer?
ENST00000302262.7:c.2497dup	ENSP00000305692.3:p.Thr833AsnfsTer?
ENST00000390015.7:c.2497dup	ENSP00000374665.3:p.Thr833AsnfsTer?
ENST00000573556.1:n.450dup
NM_000152.3:c.2497dup , LRG_673t1:c.2497dup	NP_000143.2:p.Thr833AsnfsTer?
NM_001079803.1:c.2497dup	NP_001073271.1:p.Thr833AsnfsTer?
NM_001079804.1:c.2497dup	NP_001073272.1:p.Thr833AsnfsTer?
XM_005257193.1:c.2497dup	XP_005257250.1:p.Thr833AsnfsTer?
XM_005257194.3:c.2497dup	XP_005257251.1:p.Thr833AsnfsTer?
NM_000152.4:c.2497dup	NP_000143.2:p.Thr833AsnfsTer?
NM_001079803.2:c.2497dup	NP_001073271.1:p.Thr833AsnfsTer?
NM_001079804.2:c.2497dup	NP_001073272.1:p.Thr833AsnfsTer?
XM_005257193.2:c.2497dup	XP_005257250.1:p.Thr833AsnfsTer?
XM_005257194.4:c.2497dup	XP_005257251.1:p.Thr833AsnfsTer?
NM_000152.5:c.2497dup MANE Select	NP_000143.2:p.Thr833AsnfsTer?
NM_001079803.3:c.2497dup	NP_001073271.1:p.Thr833AsnfsTer?
NM_001079804.3:c.2497dup	NP_001073272.1:p.Thr833AsnfsTer?