Canonical Allele Identifier: CA1723631679
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530927_87530930delinsAAAG , CM000669.2:g.87530927_87530930delinsAAAG GRCh38
NC_000007.13:g.87160243_87160246delinsAAAG , CM000669.1:g.87160243_87160246delinsAAAG GRCh37
NC_000007.12:g.86998179_86998182delinsAAAG NCBI36
NG_011513.1:g.187319_187322delinsCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+364_2685+367delinsCTTT ENSP00000265724.3:n.2685+364_2685+367delinsCTTT
ENST00000622132.5:c.2685+364_2685+367delinsCTTT MANE Select ENSP00000478255.1:n.2685+364_2685+367delinsCTTT
ENST00000265724.7:c.2685+364_2685+367delinsCTTT ENSP00000265724.3:n.2685+364_2685+367delinsCTTT
ENST00000488737.6:n.327+364_327+367delinsCTTT
ENST00000496821.5:n.313+364_313+367delinsCTTT
ENST00000543898.5:c.2493+364_2493+367delinsCTTT ENSP00000444095.1:n.2493+364_2493+367delinsCTTT
ENST00000622132.4:c.2685+364_2685+367delinsCTTT ENSP00000478255.1:n.2685+364_2685+367delinsCTTT
NM_000927.4:c.2685+364_2685+367delinsCTTT NP_000918.2:n.2685+364_2685+367delinsCTTT
NM_001348944.1:c.2685+364_2685+367delinsCTTT NP_001335873.1:n.2685+364_2685+367delinsCTTT
NM_001348945.1:c.2895+364_2895+367delinsCTTT NP_001335874.1:n.2895+364_2895+367delinsCTTT
NM_001348946.1:c.2685+364_2685+367delinsCTTT NP_001335875.1:n.2685+364_2685+367delinsCTTT
NM_001348946.2:c.2685+364_2685+367delinsCTTT MANE Select NP_001335875.1:n.2685+364_2685+367delinsCTTT
NM_000927.5:c.2685+364_2685+367delinsCTTT NP_000918.2:n.2685+364_2685+367delinsCTTT
NM_001348944.2:c.2685+364_2685+367delinsCTTT NP_001335873.1:n.2685+364_2685+367delinsCTTT
NM_001348945.2:c.2895+364_2895+367delinsCTTT NP_001335874.1:n.2895+364_2895+367delinsCTTT