Canonical Allele Identifier: CA1723579455

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87417397A= , CM000669.2:g.87417397A=	GRCh38
NC_000007.13:g.87046713A= , CM000669.1:g.87046713A=	GRCh37
NC_000007.12:g.86884649A=	NCBI36
NG_007118.1:g.68036T=
NG_007118.2:g.68036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2597T=	ENSP00000352135.3:p.Ile866=
ENST00000649586.2:c.2597T= MANE Select	ENSP00000496956.2:p.Ile866=
ENST00000265723.8:c.2597T=	ENSP00000265723.4:p.Ile866=
ENST00000358400.7:c.2597T=	ENSP00000351172.3:p.Ile866=
ENST00000359206.7:c.2597T=	ENSP00000352135.3:p.Ile866=
ENST00000453593.5:c.2597T=	ENSP00000392983.1:p.Ile866=
NM_000443.3:c.2597T=	NP_000434.1:p.Ile866=
NM_018849.2:c.2597T=	NP_061337.1:p.Ile866=
NM_018850.2:c.2597T=	NP_061338.1:p.Ile866=
XM_011516308.1:c.2597T=	XP_011514610.1:p.Ile866=
XM_011516309.1:c.2597T=	XP_011514611.1:p.Ile866=
XM_011516310.1:c.2492T=	XP_011514612.1:p.Ile831=
XM_011516311.1:c.2597T=	XP_011514613.1:p.Ile866=
XM_011516312.1:c.2597T=	XP_011514614.1:p.Ile866=
XM_011516313.1:c.2597T=	XP_011514615.1:p.Ile866=
XM_011516314.1:c.2618T=	XP_011514616.1:p.Ile873=
XM_011516315.1:c.1937T=	XP_011514617.1:p.Ile646=
XR_927478.1:n.2693T=
XM_011516308.3:c.2867T=	XP_011514610.3:p.Ile956=
XM_011516309.3:c.2867T=	XP_011514611.3:p.Ile956=
XM_011516310.3:c.2762T=	XP_011514612.3:p.Ile921=
XM_011516311.3:c.2867T=	XP_011514613.3:p.Ile956=
XM_011516312.3:c.2867T=	XP_011514614.3:p.Ile956=
XM_011516313.3:c.2867T=	XP_011514615.2:p.Ile956=
XM_011516315.3:c.1937T=	XP_011514617.2:p.Ile646=
XM_017012323.2:c.2597T=	XP_016867812.1:p.Ile866=
XR_001744809.2:n.3368T=
NM_000443.4:c.2597T= MANE Select	NP_000434.1:p.Ile866=
NM_018849.3:c.2597T=	NP_061337.1:p.Ile866=
NM_018850.3:c.2597T=	NP_061338.1:p.Ile866=