Canonical Allele Identifier: CA1723572981

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87411862_87411863delinsGA , CM000669.2:g.87411862_87411863delinsGA	GRCh38
NC_000007.13:g.87041178_87041179delinsGA , CM000669.1:g.87041178_87041179delinsGA	GRCh37
NC_000007.12:g.86879114_86879115delinsGA	NCBI36
NG_007118.1:g.73570_73571delinsTC
NG_007118.2:g.73570_73571delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2924+30_2924+31delinsTC	ENSP00000352135.3:n.2924+30_2924+31delinsTC
ENST00000649586.2:c.2924+30_2924+31delinsTC MANE Select	ENSP00000496956.2:n.2924+30_2924+31delinsTC
ENST00000265723.8:c.2924+30_2924+31delinsTC	ENSP00000265723.4:n.2924+30_2924+31delinsTC
ENST00000358400.7:c.2783+1754_2783+1755delinsTC	ENSP00000351172.3:n.2783+1754_2783+1755delinsTC
ENST00000359206.7:c.2924+30_2924+31delinsTC	ENSP00000352135.3:n.2924+30_2924+31delinsTC
ENST00000453593.5:c.2783+1754_2783+1755delinsTC	ENSP00000392983.1:n.2783+1754_2783+1755delinsTC
NM_000443.3:c.2924+30_2924+31delinsTC	NP_000434.1:n.2924+30_2924+31delinsTC
NM_018849.2:c.2924+30_2924+31delinsTC	NP_061337.1:n.2924+30_2924+31delinsTC
NM_018850.2:c.2783+1754_2783+1755delinsTC	NP_061338.1:n.2783+1754_2783+1755delinsTC
XM_011516308.1:c.2924+30_2924+31delinsTC	XP_011514610.1:n.2924+30_2924+31delinsTC
XM_011516309.1:c.2924+30_2924+31delinsTC	XP_011514611.1:n.2924+30_2924+31delinsTC
XM_011516310.1:c.2819+30_2819+31delinsTC	XP_011514612.1:n.2819+30_2819+31delinsTC
XM_011516311.1:c.2795+30_2795+31delinsTC	XP_011514613.1:n.2795+30_2795+31delinsTC
XM_011516312.1:c.2783+1754_2783+1755delinsTC	XP_011514614.1:n.2783+1754_2783+1755delinsTC
XM_011516313.1:c.2783+1754_2783+1755delinsTC	XP_011514615.1:n.2783+1754_2783+1755delinsTC
XM_011516314.1:c.2945+30_2945+31delinsTC	XP_011514616.1:n.2945+30_2945+31delinsTC
XM_011516315.1:c.2264+30_2264+31delinsTC	XP_011514617.1:n.2264+30_2264+31delinsTC
XR_927478.1:n.2779-2471_2779-2470delinsTC
XM_011516308.3:c.3194+30_3194+31delinsTC	XP_011514610.3:n.3194+30_3194+31delinsTC
XM_011516309.3:c.3194+30_3194+31delinsTC	XP_011514611.3:n.3194+30_3194+31delinsTC
XM_011516310.3:c.3089+30_3089+31delinsTC	XP_011514612.3:n.3089+30_3089+31delinsTC
XM_011516311.3:c.3065+30_3065+31delinsTC	XP_011514613.3:n.3065+30_3065+31delinsTC
XM_011516312.3:c.3053+1754_3053+1755delinsTC	XP_011514614.3:n.3053+1754_3053+1755delinsTC
XM_011516313.3:c.3053+1754_3053+1755delinsTC	XP_011514615.2:n.3053+1754_3053+1755delinsTC
XM_011516315.3:c.2264+30_2264+31delinsTC	XP_011514617.2:n.2264+30_2264+31delinsTC
XM_017012323.2:c.2924+30_2924+31delinsTC	XP_016867812.1:n.2924+30_2924+31delinsTC
XR_001744809.2:n.3454-2471_3454-2470delinsTC
NM_000443.4:c.2924+30_2924+31delinsTC MANE Select	NP_000434.1:n.2924+30_2924+31delinsTC
NM_018849.3:c.2924+30_2924+31delinsTC	NP_061337.1:n.2924+30_2924+31delinsTC
NM_018850.3:c.2783+1754_2783+1755delinsTC	NP_061338.1:n.2783+1754_2783+1755delinsTC