Allele Registry

HGVS	Genome Assembly
NC_000017.11:g.80108570_80108573delinsAGGT , CM000679.2:g.80108570_80108573delinsAGGT	GRCh38
NC_000017.10:g.78082369_78082372delinsAGGT , CM000679.1:g.78082369_78082372delinsAGGT	GRCh37
NC_000017.9:g.75696964_75696967delinsAGGT	NCBI36
NG_009822.1:g.12015_12018delinsAGGT , LRG_673:g.12015_12018delinsAGGT

HGVS	Amino-acid Change
ENST00000570803.6:c.1157_1160delinsAGGT	ENSP00000460543.2:p.Gln386=
ENST00000572080.2:c.1157_1160delinsAGGT	ENSP00000459972.2:p.Gln386=
ENST00000577106.6:c.1157_1160delinsAGGT	ENSP00000458306.2:p.Gln386=
ENST00000302262.8:c.1157_1160delinsAGGT MANE Select	ENSP00000305692.3:p.Gln386=
ENST00000302262.7:c.1157_1160delinsAGGT	ENSP00000305692.3:p.Gln386=
ENST00000390015.7:c.1157_1160delinsAGGT	ENSP00000374665.3:p.Gln386=
NM_000152.3:c.1157_1160delinsAGGT , LRG_673t1:c.1157_1160delinsAGGT	NP_000143.2:p.Gln386=
NM_001079803.1:c.1157_1160delinsAGGT	NP_001073271.1:p.Gln386=
NM_001079804.1:c.1157_1160delinsAGGT	NP_001073272.1:p.Gln386=
XM_005257193.1:c.1157_1160delinsAGGT	XP_005257250.1:p.Gln386=
XM_005257194.3:c.1157_1160delinsAGGT	XP_005257251.1:p.Gln386=
NM_000152.4:c.1157_1160delinsAGGT	NP_000143.2:p.Gln386=
NM_001079803.2:c.1157_1160delinsAGGT	NP_001073271.1:p.Gln386=
NM_001079804.2:c.1157_1160delinsAGGT	NP_001073272.1:p.Gln386=
XM_005257193.2:c.1157_1160delinsAGGT	XP_005257250.1:p.Gln386=
XM_005257194.4:c.1157_1160delinsAGGT	XP_005257251.1:p.Gln386=
NM_000152.5:c.1157_1160delinsAGGT MANE Select	NP_000143.2:p.Gln386=
NM_001079803.3:c.1157_1160delinsAGGT	NP_001073271.1:p.Gln386=
NM_001079804.3:c.1157_1160delinsAGGT	NP_001073272.1:p.Gln386=