Canonical Allele Identifier: CA1104138156
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87562769_87562780dup , CM000669.2:g.87562769_87562780dup GRCh38
NC_000007.13:g.87192085_87192096dup , CM000669.1:g.87192085_87192096dup GRCh37
NC_000007.12:g.87030021_87030032dup NCBI36
NG_011513.1:g.155474_155485dup

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.703-1388_703-1377dup ENSP00000265724.3:n.703-1388_703-1377dup
ENST00000622132.5:c.703-1388_703-1377dup MANE Select ENSP00000478255.1:n.703-1388_703-1377dup
ENST00000265724.7:c.703-1388_703-1377dup ENSP00000265724.3:n.703-1388_703-1377dup
ENST00000543898.5:c.511-1388_511-1377dup ENSP00000444095.1:n.511-1388_511-1377dup
ENST00000622132.4:c.703-1388_703-1377dup ENSP00000478255.1:n.703-1388_703-1377dup
NM_000927.4:c.703-1388_703-1377dup NP_000918.2:n.703-1388_703-1377dup
NM_001348944.1:c.703-1388_703-1377dup NP_001335873.1:n.703-1388_703-1377dup
NM_001348945.1:c.913-1388_913-1377dup NP_001335874.1:n.913-1388_913-1377dup
NM_001348946.1:c.703-1388_703-1377dup NP_001335875.1:n.703-1388_703-1377dup
NM_001348946.2:c.703-1388_703-1377dup MANE Select NP_001335875.1:n.703-1388_703-1377dup
NM_000927.5:c.703-1388_703-1377dup NP_000918.2:n.703-1388_703-1377dup
NM_001348944.2:c.703-1388_703-1377dup NP_001335873.1:n.703-1388_703-1377dup
NM_001348945.2:c.913-1388_913-1377dup NP_001335874.1:n.913-1388_913-1377dup