Canonical Allele Identifier: CA1723651690
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87550333_87550335delinsTCA , CM000669.2:g.87550333_87550335delinsTCA GRCh38
NC_000007.13:g.87179649_87179651delinsTCA , CM000669.1:g.87179649_87179651delinsTCA GRCh37
NC_000007.12:g.87017585_87017587delinsTCA NCBI36
NG_011513.1:g.167914_167916delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1225-39_1225-37delinsTGA ENSP00000265724.3:n.1225-39_1225-37delinsTGA
ENST00000622132.5:c.1225-39_1225-37delinsTGA MANE Select ENSP00000478255.1:n.1225-39_1225-37delinsTGA
ENST00000265724.7:c.1225-39_1225-37delinsTGA ENSP00000265724.3:n.1225-39_1225-37delinsTGA
ENST00000543898.5:c.1033-39_1033-37delinsTGA ENSP00000444095.1:n.1033-39_1033-37delinsTGA
ENST00000622132.4:c.1225-39_1225-37delinsTGA ENSP00000478255.1:n.1225-39_1225-37delinsTGA
NM_000927.4:c.1225-39_1225-37delinsTGA NP_000918.2:n.1225-39_1225-37delinsTGA
NM_001348944.1:c.1225-39_1225-37delinsTGA NP_001335873.1:n.1225-39_1225-37delinsTGA
NM_001348945.1:c.1435-39_1435-37delinsTGA NP_001335874.1:n.1435-39_1435-37delinsTGA
NM_001348946.1:c.1225-39_1225-37delinsTGA NP_001335875.1:n.1225-39_1225-37delinsTGA
NM_001348946.2:c.1225-39_1225-37delinsTGA MANE Select NP_001335875.1:n.1225-39_1225-37delinsTGA
NM_000927.5:c.1225-39_1225-37delinsTGA NP_000918.2:n.1225-39_1225-37delinsTGA
NM_001348944.2:c.1225-39_1225-37delinsTGA NP_001335873.1:n.1225-39_1225-37delinsTGA
NM_001348945.2:c.1435-39_1435-37delinsTGA NP_001335874.1:n.1435-39_1435-37delinsTGA