Canonical Allele Identifier: CA1723580042

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87417725_87417726delinsGC , CM000669.2:g.87417725_87417726delinsGC	GRCh38
NC_000007.13:g.87047041_87047042delinsGC , CM000669.1:g.87047041_87047042delinsGC	GRCh37
NC_000007.12:g.86884977_86884978delinsGC	NCBI36
NG_007118.1:g.67707_67708delinsGC
NG_007118.2:g.67707_67708delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2479-211_2479-210delinsGC	ENSP00000352135.3:n.2479-211_2479-210delinsGC
ENST00000649586.2:c.2479-211_2479-210delinsGC MANE Select	ENSP00000496956.2:n.2479-211_2479-210delinsGC
ENST00000265723.8:c.2479-211_2479-210delinsGC	ENSP00000265723.4:n.2479-211_2479-210delinsGC
ENST00000358400.7:c.2479-211_2479-210delinsGC	ENSP00000351172.3:n.2479-211_2479-210delinsGC
ENST00000359206.7:c.2479-211_2479-210delinsGC	ENSP00000352135.3:n.2479-211_2479-210delinsGC
ENST00000453593.5:c.2479-211_2479-210delinsGC	ENSP00000392983.1:n.2479-211_2479-210delinsGC
NM_000443.3:c.2479-211_2479-210delinsGC	NP_000434.1:n.2479-211_2479-210delinsGC
NM_018849.2:c.2479-211_2479-210delinsGC	NP_061337.1:n.2479-211_2479-210delinsGC
NM_018850.2:c.2479-211_2479-210delinsGC	NP_061338.1:n.2479-211_2479-210delinsGC
XM_011516308.1:c.2479-211_2479-210delinsGC	XP_011514610.1:n.2479-211_2479-210delinsGC
XM_011516309.1:c.2479-211_2479-210delinsGC	XP_011514611.1:n.2479-211_2479-210delinsGC
XM_011516310.1:c.2374-211_2374-210delinsGC	XP_011514612.1:n.2374-211_2374-210delinsGC
XM_011516311.1:c.2479-211_2479-210delinsGC	XP_011514613.1:n.2479-211_2479-210delinsGC
XM_011516312.1:c.2479-211_2479-210delinsGC	XP_011514614.1:n.2479-211_2479-210delinsGC
XM_011516313.1:c.2479-211_2479-210delinsGC	XP_011514615.1:n.2479-211_2479-210delinsGC
XM_011516314.1:c.2500-211_2500-210delinsGC	XP_011514616.1:n.2500-211_2500-210delinsGC
XM_011516315.1:c.1819-211_1819-210delinsGC	XP_011514617.1:n.1819-211_1819-210delinsGC
XR_927478.1:n.2575-211_2575-210delinsGC
XM_011516308.3:c.2749-211_2749-210delinsGC	XP_011514610.3:n.2749-211_2749-210delinsGC
XM_011516309.3:c.2749-211_2749-210delinsGC	XP_011514611.3:n.2749-211_2749-210delinsGC
XM_011516310.3:c.2644-211_2644-210delinsGC	XP_011514612.3:n.2644-211_2644-210delinsGC
XM_011516311.3:c.2749-211_2749-210delinsGC	XP_011514613.3:n.2749-211_2749-210delinsGC
XM_011516312.3:c.2749-211_2749-210delinsGC	XP_011514614.3:n.2749-211_2749-210delinsGC
XM_011516313.3:c.2749-211_2749-210delinsGC	XP_011514615.2:n.2749-211_2749-210delinsGC
XM_011516315.3:c.1819-211_1819-210delinsGC	XP_011514617.2:n.1819-211_1819-210delinsGC
XM_017012323.2:c.2479-211_2479-210delinsGC	XP_016867812.1:n.2479-211_2479-210delinsGC
XR_001744809.2:n.3250-211_3250-210delinsGC
NM_000443.4:c.2479-211_2479-210delinsGC MANE Select	NP_000434.1:n.2479-211_2479-210delinsGC
NM_018849.3:c.2479-211_2479-210delinsGC	NP_061337.1:n.2479-211_2479-210delinsGC
NM_018850.3:c.2479-211_2479-210delinsGC	NP_061338.1:n.2479-211_2479-210delinsGC