Canonical Allele Identifier: CA1104138120
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87562759_87562762dup , CM000669.2:g.87562759_87562762dup GRCh38
NC_000007.13:g.87192075_87192078dup , CM000669.1:g.87192075_87192078dup GRCh37
NC_000007.12:g.87030011_87030014dup NCBI36
NG_011513.1:g.155487_155490dup

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.703-1375_703-1372dup ENSP00000265724.3:n.703-1375_703-1372dup
ENST00000622132.5:c.703-1375_703-1372dup MANE Select ENSP00000478255.1:n.703-1375_703-1372dup
ENST00000265724.7:c.703-1375_703-1372dup ENSP00000265724.3:n.703-1375_703-1372dup
ENST00000543898.5:c.511-1375_511-1372dup ENSP00000444095.1:n.511-1375_511-1372dup
ENST00000622132.4:c.703-1375_703-1372dup ENSP00000478255.1:n.703-1375_703-1372dup
NM_000927.4:c.703-1375_703-1372dup NP_000918.2:n.703-1375_703-1372dup
NM_001348944.1:c.703-1375_703-1372dup NP_001335873.1:n.703-1375_703-1372dup
NM_001348945.1:c.913-1375_913-1372dup NP_001335874.1:n.913-1375_913-1372dup
NM_001348946.1:c.703-1375_703-1372dup NP_001335875.1:n.703-1375_703-1372dup
NM_001348946.2:c.703-1375_703-1372dup MANE Select NP_001335875.1:n.703-1375_703-1372dup
NM_000927.5:c.703-1375_703-1372dup NP_000918.2:n.703-1375_703-1372dup
NM_001348944.2:c.703-1375_703-1372dup NP_001335873.1:n.703-1375_703-1372dup
NM_001348945.2:c.913-1375_913-1372dup NP_001335874.1:n.913-1375_913-1372dup