Canonical Allele Identifier: CA1104138111
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87562757_87562758insA , CM000669.2:g.87562757_87562758insA GRCh38
NC_000007.13:g.87192073_87192074insA , CM000669.1:g.87192073_87192074insA GRCh37
NC_000007.12:g.87030009_87030010insA NCBI36
NG_011513.1:g.155491_155492insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.703-1371_703-1370insT ENSP00000265724.3:n.703-1371_703-1370insT
ENST00000622132.5:c.703-1371_703-1370insT MANE Select ENSP00000478255.1:n.703-1371_703-1370insT
ENST00000265724.7:c.703-1371_703-1370insT ENSP00000265724.3:n.703-1371_703-1370insT
ENST00000543898.5:c.511-1371_511-1370insT ENSP00000444095.1:n.511-1371_511-1370insT
ENST00000622132.4:c.703-1371_703-1370insT ENSP00000478255.1:n.703-1371_703-1370insT
NM_000927.4:c.703-1371_703-1370insT NP_000918.2:n.703-1371_703-1370insT
NM_001348944.1:c.703-1371_703-1370insT NP_001335873.1:n.703-1371_703-1370insT
NM_001348945.1:c.913-1371_913-1370insT NP_001335874.1:n.913-1371_913-1370insT
NM_001348946.1:c.703-1371_703-1370insT NP_001335875.1:n.703-1371_703-1370insT
NM_001348946.2:c.703-1371_703-1370insT MANE Select NP_001335875.1:n.703-1371_703-1370insT
NM_000927.5:c.703-1371_703-1370insT NP_000918.2:n.703-1371_703-1370insT
NM_001348944.2:c.703-1371_703-1370insT NP_001335873.1:n.703-1371_703-1370insT
NM_001348945.2:c.913-1371_913-1370insT NP_001335874.1:n.913-1371_913-1370insT