Canonical Allele Identifier: CA1723587104

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402205A= , CM000669.2:g.87402205A=	GRCh38
NC_000007.13:g.87031521A= , CM000669.1:g.87031521A=	GRCh37
NC_000007.12:g.86869457A=	NCBI36
NG_007118.1:g.83228T=
NG_007118.2:g.83228T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3731T=	ENSP00000352135.3:p.Val1244=
ENST00000649586.2:c.3731T= MANE Select	ENSP00000496956.2:p.Val1244=
ENST00000265723.8:c.3752T=	ENSP00000265723.4:p.Val1251=
ENST00000358400.7:c.3590T=	ENSP00000351172.3:p.Val1197=
ENST00000359206.7:c.3731T=	ENSP00000352135.3:p.Val1244=
ENST00000440025.1:c.165T=
ENST00000453593.5:c.3590T=	ENSP00000392983.1:p.Val1197=
ENST00000467983.1:n.343T=
NM_000443.3:c.3731T=	NP_000434.1:p.Val1244=
NM_018849.2:c.3752T=	NP_061337.1:p.Val1251=
NM_018850.2:c.3590T=	NP_061338.1:p.Val1197=
XM_011516308.1:c.3752T=	XP_011514610.1:p.Val1251=
XM_011516309.1:c.3731T=	XP_011514611.1:p.Val1244=
XM_011516310.1:c.3647T=	XP_011514612.1:p.Val1216=
XM_011516311.1:c.3623T=	XP_011514613.1:p.Val1208=
XM_011516312.1:c.3611T=	XP_011514614.1:p.Val1204=
XM_011516313.1:c.3590T=	XP_011514615.1:p.Val1197=
XM_011516314.1:c.3773T=	XP_011514616.1:p.Val1258=
XM_011516315.1:c.3092T=	XP_011514617.1:p.Val1031=
XM_011516308.3:c.4022T=	XP_011514610.3:p.Val1341=
XM_011516309.3:c.4001T=	XP_011514611.3:p.Val1334=
XM_011516310.3:c.3917T=	XP_011514612.3:p.Val1306=
XM_011516311.3:c.3893T=	XP_011514613.3:p.Val1298=
XM_011516312.3:c.3881T=	XP_011514614.3:p.Val1294=
XM_011516313.3:c.3860T=	XP_011514615.2:p.Val1287=
XM_011516315.3:c.3092T=	XP_011514617.2:p.Val1031=
XM_017012323.2:c.3752T=	XP_016867812.1:p.Val1251=
XR_001744809.2:n.4260T=
NM_000443.4:c.3731T= MANE Select	NP_000434.1:p.Val1244=
NM_018849.3:c.3752T=	NP_061337.1:p.Val1251=
NM_018850.3:c.3590T=	NP_061338.1:p.Val1197=