Canonical Allele Identifier: CA368053774
Gene: ABCB4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.87452901del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87452902del , CM000669.2:g.87452902del GRCh38
NC_000007.13:g.87082218del , CM000669.1:g.87082218del GRCh37
NC_000007.12:g.86920154del NCBI36
NG_007118.1:g.32532del
NG_007118.2:g.32532del

Transcript Alleles

HGVS Amino-acid change
ENST00000359206.8:c.536+43del ENSP00000352135.3:n.536+43del
ENST00000643670.1:c.479+43del ENSP00000496629.1:n.479+43del
ENST00000644106.1:c.536+43del ENSP00000493477.1:n.536+43del
ENST00000649586.2:c.536+43del MANE Select ENSP00000496956.2:n.536+43del
ENST00000265723.8:c.536+43del ENSP00000265723.4:n.536+43del
ENST00000358400.7:c.536+43del ENSP00000351172.3:n.536+43del
ENST00000359206.7:c.536+43del ENSP00000352135.3:n.536+43del
ENST00000453593.5:c.536+43del ENSP00000392983.1:n.536+43del
ENST00000473795.1:n.586del
NM_000443.3:c.536+43del NP_000434.1:n.536+43del
NM_018849.2:c.536+43del NP_061337.1:n.536+43del
NM_018850.2:c.536+43del NP_061338.1:n.536+43del
XM_011516308.1:c.536+43del XP_011514610.1:n.536+43del
XM_011516309.1:c.536+43del XP_011514611.1:n.536+43del
XM_011516310.1:c.536+43del XP_011514612.1:n.536+43del
XM_011516311.1:c.536+43del XP_011514613.1:n.536+43del
XM_011516312.1:c.536+43del XP_011514614.1:n.536+43del
XM_011516313.1:c.536+43del XP_011514615.1:n.536+43del
XM_011516314.1:c.557+43del XP_011514616.1:n.557+43del
XM_011516315.1:c.-48+43del XP_011514617.1:n.-48+43del
XR_927478.1:n.632+43del
XM_011516308.3:c.806+43del XP_011514610.3:n.806+43del
XM_011516309.3:c.806+43del XP_011514611.3:n.806+43del
XM_011516310.3:c.806+43del XP_011514612.3:n.806+43del
XM_011516311.3:c.806+43del XP_011514613.3:n.806+43del
XM_011516312.3:c.806+43del XP_011514614.3:n.806+43del
XM_011516313.3:c.806+43del XP_011514615.2:n.806+43del
XM_011516315.3:c.-48+43del XP_011514617.2:n.-48+43del
XM_017012323.2:c.536+43del XP_016867812.1:n.536+43del
XR_001744809.2:n.1307+43del
XR_001744810.2:n.1302+43del
NM_000443.4:c.536+43del MANE Select NP_000434.1:n.536+43del
NM_018849.3:c.536+43del NP_061337.1:n.536+43del
NM_018850.3:c.536+43del NP_061338.1:n.536+43del