Canonical Allele Identifier: CA368038578
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87439762C>G , CM000669.2:g.87439762C>G GRCh38
NC_000007.13:g.87069078C>G , CM000669.1:g.87069078C>G GRCh37
NC_000007.12:g.86907014C>G NCBI36
NG_007118.1:g.45671G>C
NG_007118.2:g.45671G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.1636G>C ENSP00000352135.3:p.Ala546Pro
ENST00000643670.1:c.1652G>C ENSP00000496629.1:n.1652G>C
ENST00000644106.1:c.*1173G>C ENSP00000493477.1:n.*1173G>C
ENST00000649586.2:c.1636G>C MANE Select ENSP00000496956.2:p.Ala546Pro
ENST00000265723.8:c.1636G>C ENSP00000265723.4:p.Ala546Pro
ENST00000358400.7:c.1636G>C ENSP00000351172.3:p.Ala546Pro
ENST00000359206.7:c.1636G>C ENSP00000352135.3:p.Ala546Pro
ENST00000453593.5:c.1636G>C ENSP00000392983.1:p.Ala546Pro
NM_000443.3:c.1636G>C NP_000434.1:p.Ala546Pro
NM_018849.2:c.1636G>C NP_061337.1:p.Ala546Pro
NM_018850.2:c.1636G>C NP_061338.1:p.Ala546Pro
XM_011516308.1:c.1636G>C XP_011514610.1:p.Ala546Pro
XM_011516309.1:c.1636G>C XP_011514611.1:p.Ala546Pro
XM_011516310.1:c.1636G>C XP_011514612.1:p.Ala546Pro
XM_011516311.1:c.1636G>C XP_011514613.1:p.Ala546Pro
XM_011516312.1:c.1636G>C XP_011514614.1:p.Ala546Pro
XM_011516313.1:c.1636G>C XP_011514615.1:p.Ala546Pro
XM_011516314.1:c.1657G>C XP_011514616.1:p.Ala553Pro
XM_011516315.1:c.976G>C XP_011514617.1:p.Ala326Pro
XR_927478.1:n.1732G>C
XM_011516308.3:c.1906G>C XP_011514610.3:p.Ala636Pro
XM_011516309.3:c.1906G>C XP_011514611.3:p.Ala636Pro
XM_011516310.3:c.1906G>C XP_011514612.3:p.Ala636Pro
XM_011516311.3:c.1906G>C XP_011514613.3:p.Ala636Pro
XM_011516312.3:c.1906G>C XP_011514614.3:p.Ala636Pro
XM_011516313.3:c.1906G>C XP_011514615.2:p.Ala636Pro
XM_011516315.3:c.976G>C XP_011514617.2:p.Ala326Pro
XM_017012323.2:c.1636G>C XP_016867812.1:p.Ala546Pro
XR_001744809.2:n.2407G>C
XR_001744810.2:n.2402G>C
NM_000443.4:c.1636G>C MANE Select NP_000434.1:p.Ala546Pro
NM_018849.3:c.1636G>C NP_061337.1:p.Ala546Pro
NM_018850.3:c.1636G>C NP_061338.1:p.Ala546Pro