Canonical Allele Identifier: CA1723651372
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87550123_87550125delinsATG , CM000669.2:g.87550123_87550125delinsATG GRCh38
NC_000007.13:g.87179439_87179441delinsATG , CM000669.1:g.87179439_87179441delinsATG GRCh37
NC_000007.12:g.87017375_87017377delinsATG NCBI36
NG_011513.1:g.168124_168126delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1350+46_1350+48delinsCAT ENSP00000265724.3:n.1350+46_1350+48delinsCAT
ENST00000622132.5:c.1350+46_1350+48delinsCAT MANE Select ENSP00000478255.1:n.1350+46_1350+48delinsCAT
ENST00000265724.7:c.1350+46_1350+48delinsCAT ENSP00000265724.3:n.1350+46_1350+48delinsCAT
ENST00000482527.1:n.34_36delinsCAT
ENST00000543898.5:c.1158+46_1158+48delinsCAT ENSP00000444095.1:n.1158+46_1158+48delinsCAT
ENST00000622132.4:c.1350+46_1350+48delinsCAT ENSP00000478255.1:n.1350+46_1350+48delinsCAT
NM_000927.4:c.1350+46_1350+48delinsCAT NP_000918.2:n.1350+46_1350+48delinsCAT
NM_001348944.1:c.1350+46_1350+48delinsCAT NP_001335873.1:n.1350+46_1350+48delinsCAT
NM_001348945.1:c.1560+46_1560+48delinsCAT NP_001335874.1:n.1560+46_1560+48delinsCAT
NM_001348946.1:c.1350+46_1350+48delinsCAT NP_001335875.1:n.1350+46_1350+48delinsCAT
NM_001348946.2:c.1350+46_1350+48delinsCAT MANE Select NP_001335875.1:n.1350+46_1350+48delinsCAT
NM_000927.5:c.1350+46_1350+48delinsCAT NP_000918.2:n.1350+46_1350+48delinsCAT
NM_001348944.2:c.1350+46_1350+48delinsCAT NP_001335873.1:n.1350+46_1350+48delinsCAT
NM_001348945.2:c.1560+46_1560+48delinsCAT NP_001335874.1:n.1560+46_1560+48delinsCAT