Canonical Allele Identifier: CA368038615
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87439768C>A , CM000669.2:g.87439768C>A GRCh38
NC_000007.13:g.87069084C>A , CM000669.1:g.87069084C>A GRCh37
NC_000007.12:g.86907020C>A NCBI36
NG_007118.1:g.45665G>T
NG_007118.2:g.45665G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359206.8:c.1630G>T ENSP00000352135.3:p.Ala544Ser
ENST00000643670.1:c.1646G>T ENSP00000496629.1:n.1646G>T
ENST00000644106.1:c.*1167G>T ENSP00000493477.1:n.*1167G>T
ENST00000649586.2:c.1630G>T MANE Select ENSP00000496956.2:p.Ala544Ser
ENST00000265723.8:c.1630G>T ENSP00000265723.4:p.Ala544Ser
ENST00000358400.7:c.1630G>T ENSP00000351172.3:p.Ala544Ser
ENST00000359206.7:c.1630G>T ENSP00000352135.3:p.Ala544Ser
ENST00000453593.5:c.1630G>T ENSP00000392983.1:p.Ala544Ser
NM_000443.3:c.1630G>T NP_000434.1:p.Ala544Ser
NM_018849.2:c.1630G>T NP_061337.1:p.Ala544Ser
NM_018850.2:c.1630G>T NP_061338.1:p.Ala544Ser
XM_011516308.1:c.1630G>T XP_011514610.1:p.Ala544Ser
XM_011516309.1:c.1630G>T XP_011514611.1:p.Ala544Ser
XM_011516310.1:c.1630G>T XP_011514612.1:p.Ala544Ser
XM_011516311.1:c.1630G>T XP_011514613.1:p.Ala544Ser
XM_011516312.1:c.1630G>T XP_011514614.1:p.Ala544Ser
XM_011516313.1:c.1630G>T XP_011514615.1:p.Ala544Ser
XM_011516314.1:c.1651G>T XP_011514616.1:p.Ala551Ser
XM_011516315.1:c.970G>T XP_011514617.1:p.Ala324Ser
XR_927478.1:n.1726G>T
XM_011516308.3:c.1900G>T XP_011514610.3:p.Ala634Ser
XM_011516309.3:c.1900G>T XP_011514611.3:p.Ala634Ser
XM_011516310.3:c.1900G>T XP_011514612.3:p.Ala634Ser
XM_011516311.3:c.1900G>T XP_011514613.3:p.Ala634Ser
XM_011516312.3:c.1900G>T XP_011514614.3:p.Ala634Ser
XM_011516313.3:c.1900G>T XP_011514615.2:p.Ala634Ser
XM_011516315.3:c.970G>T XP_011514617.2:p.Ala324Ser
XM_017012323.2:c.1630G>T XP_016867812.1:p.Ala544Ser
XR_001744809.2:n.2401G>T
XR_001744810.2:n.2396G>T
NM_000443.4:c.1630G>T MANE Select NP_000434.1:p.Ala544Ser
NM_018849.3:c.1630G>T NP_061337.1:p.Ala544Ser
NM_018850.3:c.1630G>T NP_061338.1:p.Ala544Ser