Canonical Allele Identifier: CA1723579119

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87452906_87452907delinsAT , CM000669.2:g.87452906_87452907delinsAT	GRCh38
NC_000007.13:g.87082222_87082223delinsAT , CM000669.1:g.87082222_87082223delinsAT	GRCh37
NC_000007.12:g.86920158_86920159delinsAT	NCBI36
NG_007118.1:g.32526_32527delinsAT
NG_007118.2:g.32526_32527delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.536+37_536+38delinsAT	ENSP00000352135.3:n.536+37_536+38delinsAT...
ENST00000643670.1:c.479+37_479+38delinsAT	ENSP00000496629.1:n.479+37_479+38delinsAT...
ENST00000644106.1:c.536+37_536+38delinsAT	ENSP00000493477.1:n.536+37_536+38delinsAT...
ENST00000649586.2:c.536+37_536+38delinsAT MANE Select	ENSP00000496956.2:n.536+37_536+38delinsAT...
ENST00000265723.8:c.536+37_536+38delinsAT	ENSP00000265723.4:n.536+37_536+38delinsAT...
ENST00000358400.7:c.536+37_536+38delinsAT	ENSP00000351172.3:n.536+37_536+38delinsAT...
ENST00000359206.7:c.536+37_536+38delinsAT	ENSP00000352135.3:n.536+37_536+38delinsAT...
ENST00000453593.5:c.536+37_536+38delinsAT	ENSP00000392983.1:n.536+37_536+38delinsAT...
ENST00000473795.1:n.580_581delinsAT
NM_000443.3:c.536+37_536+38delinsAT	NP_000434.1:n.536+37_536+38delinsAT
NM_018849.2:c.536+37_536+38delinsAT	NP_061337.1:n.536+37_536+38delinsAT
NM_018850.2:c.536+37_536+38delinsAT	NP_061338.1:n.536+37_536+38delinsAT
XM_011516308.1:c.536+37_536+38delinsAT	XP_011514610.1:n.536+37_536+38delinsAT
XM_011516309.1:c.536+37_536+38delinsAT	XP_011514611.1:n.536+37_536+38delinsAT
XM_011516310.1:c.536+37_536+38delinsAT	XP_011514612.1:n.536+37_536+38delinsAT
XM_011516311.1:c.536+37_536+38delinsAT	XP_011514613.1:n.536+37_536+38delinsAT
XM_011516312.1:c.536+37_536+38delinsAT	XP_011514614.1:n.536+37_536+38delinsAT
XM_011516313.1:c.536+37_536+38delinsAT	XP_011514615.1:n.536+37_536+38delinsAT
XM_011516314.1:c.557+37_557+38delinsAT	XP_011514616.1:n.557+37_557+38delinsAT
XM_011516315.1:c.-48+37_-48+38delinsAT	XP_011514617.1:n.-48+37_-48+38delinsAT
XR_927478.1:n.632+37_632+38delinsAT
XM_011516308.3:c.806+37_806+38delinsAT	XP_011514610.3:n.806+37_806+38delinsAT
XM_011516309.3:c.806+37_806+38delinsAT	XP_011514611.3:n.806+37_806+38delinsAT
XM_011516310.3:c.806+37_806+38delinsAT	XP_011514612.3:n.806+37_806+38delinsAT
XM_011516311.3:c.806+37_806+38delinsAT	XP_011514613.3:n.806+37_806+38delinsAT
XM_011516312.3:c.806+37_806+38delinsAT	XP_011514614.3:n.806+37_806+38delinsAT
XM_011516313.3:c.806+37_806+38delinsAT	XP_011514615.2:n.806+37_806+38delinsAT
XM_011516315.3:c.-48+37_-48+38delinsAT	XP_011514617.2:n.-48+37_-48+38delinsAT
XM_017012323.2:c.536+37_536+38delinsAT	XP_016867812.1:n.536+37_536+38delinsAT
XR_001744809.2:n.1307+37_1307+38delinsAT
XR_001744810.2:n.1302+37_1302+38delinsAT
NM_000443.4:c.536+37_536+38delinsAT MANE Select	NP_000434.1:n.536+37_536+38delinsAT
NM_018849.3:c.536+37_536+38delinsAT	NP_061337.1:n.536+37_536+38delinsAT
NM_018850.3:c.536+37_536+38delinsAT	NP_061338.1:n.536+37_536+38delinsAT