Canonical Allele Identifier: CA1723571479

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87447018_87447021delinsTAGG , CM000669.2:g.87447018_87447021delinsTAGG	GRCh38
NC_000007.13:g.87076334_87076337delinsTAGG , CM000669.1:g.87076334_87076337delinsTAGG	GRCh37
NC_000007.12:g.86914270_86914273delinsTAGG	NCBI36
NG_007118.1:g.38412_38415delinsCCTA
NG_007118.2:g.38412_38415delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.1005+13_1005+16delinsCCTA	ENSP00000352135.3:n.1005+13_1005+16delinsCCTA
ENST00000643670.1:c.1021+13_1021+16delinsCCTA	ENSP00000496629.1:n.1021+13_1021+16delinsCCTA
ENST00000644106.1:c.*542+13_*542+16delinsCCTA	ENSP00000493477.1:n.*542+13_*542+16delinsCCTA
ENST00000649586.2:c.1005+13_1005+16delinsCCTA MANE Select	ENSP00000496956.2:n.1005+13_1005+16delinsCCTA
ENST00000265723.8:c.1005+13_1005+16delinsCCTA	ENSP00000265723.4:n.1005+13_1005+16delinsCCTA
ENST00000358400.7:c.1005+13_1005+16delinsCCTA	ENSP00000351172.3:n.1005+13_1005+16delinsCCTA
ENST00000359206.7:c.1005+13_1005+16delinsCCTA	ENSP00000352135.3:n.1005+13_1005+16delinsCCTA
ENST00000453593.5:c.1005+13_1005+16delinsCCTA	ENSP00000392983.1:n.1005+13_1005+16delinsCCTA
NM_000443.3:c.1005+13_1005+16delinsCCTA	NP_000434.1:n.1005+13_1005+16delinsCCTA
NM_018849.2:c.1005+13_1005+16delinsCCTA	NP_061337.1:n.1005+13_1005+16delinsCCTA
NM_018850.2:c.1005+13_1005+16delinsCCTA	NP_061338.1:n.1005+13_1005+16delinsCCTA
XM_011516308.1:c.1005+13_1005+16delinsCCTA	XP_011514610.1:n.1005+13_1005+16delinsCCTA
XM_011516309.1:c.1005+13_1005+16delinsCCTA	XP_011514611.1:n.1005+13_1005+16delinsCCTA
XM_011516310.1:c.1005+13_1005+16delinsCCTA	XP_011514612.1:n.1005+13_1005+16delinsCCTA
XM_011516311.1:c.1005+13_1005+16delinsCCTA	XP_011514613.1:n.1005+13_1005+16delinsCCTA
XM_011516312.1:c.1005+13_1005+16delinsCCTA	XP_011514614.1:n.1005+13_1005+16delinsCCTA
XM_011516313.1:c.1005+13_1005+16delinsCCTA	XP_011514615.1:n.1005+13_1005+16delinsCCTA
XM_011516314.1:c.1026+13_1026+16delinsCCTA	XP_011514616.1:n.1026+13_1026+16delinsCCTA
XM_011516315.1:c.345+13_345+16delinsCCTA	XP_011514617.1:n.345+13_345+16delinsCCTA
XR_927478.1:n.1101+13_1101+16delinsCCTA
XM_011516308.3:c.1275+13_1275+16delinsCCTA	XP_011514610.3:n.1275+13_1275+16delinsCCTA
XM_011516309.3:c.1275+13_1275+16delinsCCTA	XP_011514611.3:n.1275+13_1275+16delinsCCTA
XM_011516310.3:c.1275+13_1275+16delinsCCTA	XP_011514612.3:n.1275+13_1275+16delinsCCTA
XM_011516311.3:c.1275+13_1275+16delinsCCTA	XP_011514613.3:n.1275+13_1275+16delinsCCTA
XM_011516312.3:c.1275+13_1275+16delinsCCTA	XP_011514614.3:n.1275+13_1275+16delinsCCTA
XM_011516313.3:c.1275+13_1275+16delinsCCTA	XP_011514615.2:n.1275+13_1275+16delinsCCTA
XM_011516315.3:c.345+13_345+16delinsCCTA	XP_011514617.2:n.345+13_345+16delinsCCTA
XM_017012323.2:c.1005+13_1005+16delinsCCTA	XP_016867812.1:n.1005+13_1005+16delinsCCTA
XR_001744809.2:n.1776+13_1776+16delinsCCTA
XR_001744810.2:n.1771+13_1771+16delinsCCTA
NM_000443.4:c.1005+13_1005+16delinsCCTA MANE Select	NP_000434.1:n.1005+13_1005+16delinsCCTA
NM_018849.3:c.1005+13_1005+16delinsCCTA	NP_061337.1:n.1005+13_1005+16delinsCCTA
NM_018850.3:c.1005+13_1005+16delinsCCTA	NP_061338.1:n.1005+13_1005+16delinsCCTA