Canonical Allele Identifier: CA1723630870
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530785_87530801delinsAAAAGAAAGAAAGCAAG , CM000669.2:g.87530785_87530801delinsAAAAGAAAGAAAGCAAG GRCh38
NC_000007.13:g.87160101_87160117delinsAAAAGAAAGAAAGCAAG , CM000669.1:g.87160101_87160117delinsAAAAGAAAGAAAGCAAG GRCh37
NC_000007.12:g.86998037_86998053delinsAAAAGAAAGAAAGCAAG NCBI36
NG_011513.1:g.187448_187464delinsCTTGCTTTCTTTCTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT ENSP00000265724.3:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
ENST00000622132.5:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT MANE Select ENSP00000478255.1:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
ENST00000265724.7:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT ENSP00000265724.3:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
ENST00000488737.6:n.327+493_327+509delinsCTTGCTTTCTTTCTTTT
ENST00000496821.5:n.313+493_313+509delinsCTTGCTTTCTTTCTTTT
ENST00000543898.5:c.2493+493_2493+509delinsCTTGCTTTCTTTCTTTT ENSP00000444095.1:n.2493+493_2493+509delinsCTTGCTTTCTTTCTTTT
ENST00000622132.4:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT ENSP00000478255.1:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
NM_000927.4:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT NP_000918.2:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
NM_001348944.1:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT NP_001335873.1:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
NM_001348945.1:c.2895+493_2895+509delinsCTTGCTTTCTTTCTTTT NP_001335874.1:n.2895+493_2895+509delinsCTTGCTTTCTTTCTTTT
NM_001348946.1:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT NP_001335875.1:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
NM_001348946.2:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT MANE Select NP_001335875.1:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
NM_000927.5:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT NP_000918.2:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
NM_001348944.2:c.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT NP_001335873.1:n.2685+493_2685+509delinsCTTGCTTTCTTTCTTTT
NM_001348945.2:c.2895+493_2895+509delinsCTTGCTTTCTTTCTTTT NP_001335874.1:n.2895+493_2895+509delinsCTTGCTTTCTTTCTTTT