Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958028T= , CM000672.2:g.87958028T=	GRCh38
NC_000010.10:g.89717785T= , CM000672.1:g.89717785T=	GRCh37
NC_000010.9:g.89707765T=	NCBI36
NG_007466.2:g.99590T= , LRG_311:g.99590T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.801+9T=	ENSP00000514759.2:n.801+9T=
ENST00000710265.1:c.801+9T=	ENSP00000518161.1:n.801+9T=
ENST00000472832.3:c.801+9T=	ENSP00000483066.2:n.801+9T=
ENST00000688158.2:n.1536+9T=
ENST00000688922.2:c.*631+9T=	ENSP00000508742.2:n.*631+9T=
ENST00000700021.1:c.756+9T=	ENSP00000514757.1:n.756+9T=
ENST00000700022.1:c.*140+9T=	ENSP00000514758.1:n.*140+9T=
ENST00000700023.1:n.1959+9T=
ENST00000700024.1:n.2193+9T=
ENST00000700025.1:n.1570+9T=
ENST00000700026.1:n.438+9T=
ENST00000700029.1:c.635+9T=
ENST00000706954.1:c.801+9T=	ENSP00000516674.1:n.801+9T=
ENST00000706955.1:c.*836+9T=	ENSP00000516675.1:n.*836+9T=
ENST00000686459.1:c.*387+9T=	ENSP00000508909.1:n.*387+9T=
ENST00000688158.1:c.*912+9T=	ENSP00000509254.1:n.*912+9T=
ENST00000688308.1:c.801+9T=	ENSP00000508752.1:n.801+9T=
ENST00000688922.1:c.722+9T=
ENST00000693560.1:c.1320+9T=	ENSP00000509861.1:n.1320+9T=
ENST00000371953.8:c.801+9T= MANE Select	ENSP00000361021.3:n.801+9T=
ENST00000371953.7:c.801+9T=	ENSP00000361021.3:n.801+9T=
ENST00000472832.2:c.228+9T=	ENSP00000483066.1:n.228+9T=
NM_000314.5:c.801+9T=	NP_000305.3:n.801+9T=
NM_000314.6:c.801+9T=	NP_000305.3:n.801+9T=
NM_001304717.2:c.1320+9T=	NP_001291646.2:n.1320+9T=
NM_001304718.1:c.210+9T=	NP_001291647.1:n.210+9T=
XM_006717926.2:c.756+9T=	XP_006717989.1:n.756+9T=
XM_011539981.1:c.801+9T=	XP_011538283.1:n.801+9T=
XM_011539982.1:c.705+9T=	XP_011538284.1:n.705+9T=
XR_945791.1:n.1371+9T=
NM_000314.7:c.801+9T=	NP_000305.3:n.801+9T=
NM_001304717.5:c.1320+9T=	NP_001291646.4:n.1320+9T=
NM_001304718.2:c.210+9T=	NP_001291647.1:n.210+9T=
NM_000314.8:c.801+9T= MANE Select	NP_000305.3:n.801+9T=