Canonical Allele Identifier: CA1723572087

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87447334_87447335delinsAC , CM000669.2:g.87447334_87447335delinsAC	GRCh38
NC_000007.13:g.87076650_87076651delinsAC , CM000669.1:g.87076650_87076651delinsAC	GRCh37
NC_000007.12:g.86914586_86914587delinsAC	NCBI36
NG_007118.1:g.38098_38099delinsGT
NG_007118.2:g.38098_38099delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.834-130_834-129delinsGT	ENSP00000352135.3:n.834-130_834-129delinsGT
ENST00000643670.1:c.850-130_850-129delinsGT	ENSP00000496629.1:n.850-130_850-129delinsGT
ENST00000644106.1:c.*371-130_*371-129delinsGT	ENSP00000493477.1:n.*371-130_*371-129delinsGT
ENST00000649586.2:c.834-130_834-129delinsGT MANE Select	ENSP00000496956.2:n.834-130_834-129delinsGT
ENST00000265723.8:c.834-130_834-129delinsGT	ENSP00000265723.4:n.834-130_834-129delinsGT
ENST00000358400.7:c.834-130_834-129delinsGT	ENSP00000351172.3:n.834-130_834-129delinsGT
ENST00000359206.7:c.834-130_834-129delinsGT	ENSP00000352135.3:n.834-130_834-129delinsGT
ENST00000453593.5:c.834-130_834-129delinsGT	ENSP00000392983.1:n.834-130_834-129delinsGT
NM_000443.3:c.834-130_834-129delinsGT	NP_000434.1:n.834-130_834-129delinsGT
NM_018849.2:c.834-130_834-129delinsGT	NP_061337.1:n.834-130_834-129delinsGT
NM_018850.2:c.834-130_834-129delinsGT	NP_061338.1:n.834-130_834-129delinsGT
XM_011516308.1:c.834-130_834-129delinsGT	XP_011514610.1:n.834-130_834-129delinsGT
XM_011516309.1:c.834-130_834-129delinsGT	XP_011514611.1:n.834-130_834-129delinsGT
XM_011516310.1:c.834-130_834-129delinsGT	XP_011514612.1:n.834-130_834-129delinsGT
XM_011516311.1:c.834-130_834-129delinsGT	XP_011514613.1:n.834-130_834-129delinsGT
XM_011516312.1:c.834-130_834-129delinsGT	XP_011514614.1:n.834-130_834-129delinsGT
XM_011516313.1:c.834-130_834-129delinsGT	XP_011514615.1:n.834-130_834-129delinsGT
XM_011516314.1:c.855-130_855-129delinsGT	XP_011514616.1:n.855-130_855-129delinsGT
XM_011516315.1:c.174-130_174-129delinsGT	XP_011514617.1:n.174-130_174-129delinsGT
XR_927478.1:n.930-130_930-129delinsGT
XM_011516308.3:c.1104-130_1104-129delinsGT	XP_011514610.3:n.1104-130_1104-129delinsGT
XM_011516309.3:c.1104-130_1104-129delinsGT	XP_011514611.3:n.1104-130_1104-129delinsGT
XM_011516310.3:c.1104-130_1104-129delinsGT	XP_011514612.3:n.1104-130_1104-129delinsGT
XM_011516311.3:c.1104-130_1104-129delinsGT	XP_011514613.3:n.1104-130_1104-129delinsGT
XM_011516312.3:c.1104-130_1104-129delinsGT	XP_011514614.3:n.1104-130_1104-129delinsGT
XM_011516313.3:c.1104-130_1104-129delinsGT	XP_011514615.2:n.1104-130_1104-129delinsGT
XM_011516315.3:c.174-130_174-129delinsGT	XP_011514617.2:n.174-130_174-129delinsGT
XM_017012323.2:c.834-130_834-129delinsGT	XP_016867812.1:n.834-130_834-129delinsGT
XR_001744809.2:n.1605-130_1605-129delinsGT
XR_001744810.2:n.1600-130_1600-129delinsGT
NM_000443.4:c.834-130_834-129delinsGT MANE Select	NP_000434.1:n.834-130_834-129delinsGT
NM_018849.3:c.834-130_834-129delinsGT	NP_061337.1:n.834-130_834-129delinsGT
NM_018850.3:c.834-130_834-129delinsGT	NP_061338.1:n.834-130_834-129delinsGT