Canonical Allele Identifier: CA2683600172

Gene: ABCB4

Linked Data

• gnomAD v4: 7-87423794-GTTTAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87423800_87423804del , CM000669.2:g.87423800_87423804del	GRCh38
NC_000007.13:g.87053116_87053120del , CM000669.1:g.87053116_87053120del	GRCh37
NC_000007.12:g.86891052_86891056del	NCBI36
NG_007118.1:g.61634_61638del
NG_007118.2:g.61634_61638del

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.2211+107_2211+111del	ENSP00000352135.3:n.2211+107_2211+111del
ENST00000649586.2:c.2211+107_2211+111del MANE Select	ENSP00000496956.2:n.2211+107_2211+111del
ENST00000265723.8:c.2211+107_2211+111del	ENSP00000265723.4:n.2211+107_2211+111del
ENST00000358400.7:c.2211+107_2211+111del	ENSP00000351172.3:n.2211+107_2211+111del
ENST00000359206.7:c.2211+107_2211+111del	ENSP00000352135.3:n.2211+107_2211+111del
ENST00000453593.5:c.2211+107_2211+111del	ENSP00000392983.1:n.2211+107_2211+111del
ENST00000469770.1:n.522_526del
NM_000443.3:c.2211+107_2211+111del	NP_000434.1:n.2211+107_2211+111del
NM_018849.2:c.2211+107_2211+111del	NP_061337.1:n.2211+107_2211+111del
NM_018850.2:c.2211+107_2211+111del	NP_061338.1:n.2211+107_2211+111del
XM_011516308.1:c.2211+107_2211+111del	XP_011514610.1:n.2211+107_2211+111del
XM_011516309.1:c.2211+107_2211+111del	XP_011514611.1:n.2211+107_2211+111del
XM_011516310.1:c.2211+107_2211+111del	XP_011514612.1:n.2211+107_2211+111del
XM_011516311.1:c.2211+107_2211+111del	XP_011514613.1:n.2211+107_2211+111del
XM_011516312.1:c.2211+107_2211+111del	XP_011514614.1:n.2211+107_2211+111del
XM_011516313.1:c.2211+107_2211+111del	XP_011514615.1:n.2211+107_2211+111del
XM_011516314.1:c.2232+107_2232+111del	XP_011514616.1:n.2232+107_2232+111del
XM_011516315.1:c.1551+107_1551+111del	XP_011514617.1:n.1551+107_1551+111del
XR_927478.1:n.2307+107_2307+111del
XM_011516308.3:c.2481+107_2481+111del	XP_011514610.3:n.2481+107_2481+111del
XM_011516309.3:c.2481+107_2481+111del	XP_011514611.3:n.2481+107_2481+111del
XM_011516310.3:c.2481+107_2481+111del	XP_011514612.3:n.2481+107_2481+111del
XM_011516311.3:c.2481+107_2481+111del	XP_011514613.3:n.2481+107_2481+111del
XM_011516312.3:c.2481+107_2481+111del	XP_011514614.3:n.2481+107_2481+111del
XM_011516313.3:c.2481+107_2481+111del	XP_011514615.2:n.2481+107_2481+111del
XM_011516315.3:c.1551+107_1551+111del	XP_011514617.2:n.1551+107_1551+111del
XM_017012323.2:c.2211+107_2211+111del	XP_016867812.1:n.2211+107_2211+111del
XR_001744809.2:n.2982+107_2982+111del
XR_001744810.2:n.2977+107_2977+111del
NM_000443.4:c.2211+107_2211+111del MANE Select	NP_000434.1:n.2211+107_2211+111del
NM_018849.3:c.2211+107_2211+111del	NP_061337.1:n.2211+107_2211+111del
NM_018850.3:c.2211+107_2211+111del	NP_061338.1:n.2211+107_2211+111del