Canonical Allele Identifier: CA2558560546
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87532224_87532225insACT , CM000669.2:g.87532224_87532225insACT GRCh38
NC_000007.13:g.87161540_87161541insACT , CM000669.1:g.87161540_87161541insACT GRCh37
NC_000007.12:g.86999476_86999477insACT NCBI36
NG_011513.1:g.186024_186025insAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.2482-728_2482-727insAGT ENSP00000265724.3:n.2482-728_2482-727insA...
ENST00000622132.5:c.2482-728_2482-727insAGT MANE Select ENSP00000478255.1:n.2482-728_2482-727insA...
ENST00000265724.7:c.2482-728_2482-727insAGT ENSP00000265724.3:n.2482-728_2482-727insA...
ENST00000496821.5:n.110-728_110-727insAGT
ENST00000543898.5:c.2290-728_2290-727insAGT ENSP00000444095.1:n.2290-728_2290-727insA...
ENST00000622132.4:c.2482-728_2482-727insAGT ENSP00000478255.1:n.2482-728_2482-727insA...
NM_000927.4:c.2482-728_2482-727insAGT NP_000918.2:n.2482-728_2482-727insAGT
NM_001348944.1:c.2482-728_2482-727insAGT NP_001335873.1:n.2482-728_2482-727insAGT
NM_001348945.1:c.2692-728_2692-727insAGT NP_001335874.1:n.2692-728_2692-727insAGT
NM_001348946.1:c.2482-728_2482-727insAGT NP_001335875.1:n.2482-728_2482-727insAGT
NM_001348946.2:c.2482-728_2482-727insAGT MANE Select NP_001335875.1:n.2482-728_2482-727insAGT
NM_000927.5:c.2482-728_2482-727insAGT NP_000918.2:n.2482-728_2482-727insAGT
NM_001348944.2:c.2482-728_2482-727insAGT NP_001335873.1:n.2482-728_2482-727insAGT
NM_001348945.2:c.2692-728_2692-727insAGT NP_001335874.1:n.2692-728_2692-727insAGT