Canonical Allele Identifier: CA1723593059

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87431626_87431628delinsGCA , CM000669.2:g.87431626_87431628delinsGCA	GRCh38
NC_000007.13:g.87060942_87060944delinsGCA , CM000669.1:g.87060942_87060944delinsGCA	GRCh37
NC_000007.12:g.86898878_86898880delinsGCA	NCBI36
NG_007118.1:g.53805_53807delinsTGC
NG_007118.2:g.53805_53807delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.1732-63_1732-61delinsTGC	ENSP00000352135.3:n.1732-63_1732-61delinsTGC
ENST00000643670.1:c.1748-63_1748-61delinsTGC	ENSP00000496629.1:n.1748-63_1748-61delinsTGC
ENST00000644106.1:c.*1269-63_*1269-61delinsTGC	ENSP00000493477.1:n.*1269-63_*1269-61delinsTGC
ENST00000649586.2:c.1732-63_1732-61delinsTGC MANE Select	ENSP00000496956.2:n.1732-63_1732-61delinsTGC
ENST00000265723.8:c.1732-63_1732-61delinsTGC	ENSP00000265723.4:n.1732-63_1732-61delinsTGC
ENST00000358400.7:c.1732-63_1732-61delinsTGC	ENSP00000351172.3:n.1732-63_1732-61delinsTGC
ENST00000359206.7:c.1732-63_1732-61delinsTGC	ENSP00000352135.3:n.1732-63_1732-61delinsTGC
ENST00000453593.5:c.1732-63_1732-61delinsTGC	ENSP00000392983.1:n.1732-63_1732-61delinsTGC
NM_000443.3:c.1732-63_1732-61delinsTGC	NP_000434.1:n.1732-63_1732-61delinsTGC
NM_018849.2:c.1732-63_1732-61delinsTGC	NP_061337.1:n.1732-63_1732-61delinsTGC
NM_018850.2:c.1732-63_1732-61delinsTGC	NP_061338.1:n.1732-63_1732-61delinsTGC
XM_011516308.1:c.1732-63_1732-61delinsTGC	XP_011514610.1:n.1732-63_1732-61delinsTGC
XM_011516309.1:c.1732-63_1732-61delinsTGC	XP_011514611.1:n.1732-63_1732-61delinsTGC
XM_011516310.1:c.1732-63_1732-61delinsTGC	XP_011514612.1:n.1732-63_1732-61delinsTGC
XM_011516311.1:c.1732-63_1732-61delinsTGC	XP_011514613.1:n.1732-63_1732-61delinsTGC
XM_011516312.1:c.1732-63_1732-61delinsTGC	XP_011514614.1:n.1732-63_1732-61delinsTGC
XM_011516313.1:c.1732-63_1732-61delinsTGC	XP_011514615.1:n.1732-63_1732-61delinsTGC
XM_011516314.1:c.1753-63_1753-61delinsTGC	XP_011514616.1:n.1753-63_1753-61delinsTGC
XM_011516315.1:c.1072-63_1072-61delinsTGC	XP_011514617.1:n.1072-63_1072-61delinsTGC
XR_927478.1:n.1828-63_1828-61delinsTGC
XM_011516308.3:c.2002-63_2002-61delinsTGC	XP_011514610.3:n.2002-63_2002-61delinsTGC
XM_011516309.3:c.2002-63_2002-61delinsTGC	XP_011514611.3:n.2002-63_2002-61delinsTGC
XM_011516310.3:c.2002-63_2002-61delinsTGC	XP_011514612.3:n.2002-63_2002-61delinsTGC
XM_011516311.3:c.2002-63_2002-61delinsTGC	XP_011514613.3:n.2002-63_2002-61delinsTGC
XM_011516312.3:c.2002-63_2002-61delinsTGC	XP_011514614.3:n.2002-63_2002-61delinsTGC
XM_011516313.3:c.2002-63_2002-61delinsTGC	XP_011514615.2:n.2002-63_2002-61delinsTGC
XM_011516315.3:c.1072-63_1072-61delinsTGC	XP_011514617.2:n.1072-63_1072-61delinsTGC
XM_017012323.2:c.1732-63_1732-61delinsTGC	XP_016867812.1:n.1732-63_1732-61delinsTGC
XR_001744809.2:n.2503-63_2503-61delinsTGC
XR_001744810.2:n.2498-63_2498-61delinsTGC
NM_000443.4:c.1732-63_1732-61delinsTGC MANE Select	NP_000434.1:n.1732-63_1732-61delinsTGC
NM_018849.3:c.1732-63_1732-61delinsTGC	NP_061337.1:n.1732-63_1732-61delinsTGC
NM_018850.3:c.1732-63_1732-61delinsTGC	NP_061338.1:n.1732-63_1732-61delinsTGC