Canonical Allele Identifier: CA1723630873
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530785_87530793delinsAAAAGAAAG , CM000669.2:g.87530785_87530793delinsAAAAGAAAG GRCh38
NC_000007.13:g.87160101_87160109delinsAAAAGAAAG , CM000669.1:g.87160101_87160109delinsAAAAGAAAG GRCh37
NC_000007.12:g.86998037_86998045delinsAAAAGAAAG NCBI36
NG_011513.1:g.187456_187464delinsCTTTCTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+501_2685+509delinsCTTTCTTTT ENSP00000265724.3:n.2685+501_2685+509delinsCTTTCTTTT
ENST00000622132.5:c.2685+501_2685+509delinsCTTTCTTTT MANE Select ENSP00000478255.1:n.2685+501_2685+509delinsCTTTCTTTT
ENST00000265724.7:c.2685+501_2685+509delinsCTTTCTTTT ENSP00000265724.3:n.2685+501_2685+509delinsCTTTCTTTT
ENST00000488737.6:n.327+501_327+509delinsCTTTCTTTT
ENST00000496821.5:n.313+501_313+509delinsCTTTCTTTT
ENST00000543898.5:c.2493+501_2493+509delinsCTTTCTTTT ENSP00000444095.1:n.2493+501_2493+509delinsCTTTCTTTT
ENST00000622132.4:c.2685+501_2685+509delinsCTTTCTTTT ENSP00000478255.1:n.2685+501_2685+509delinsCTTTCTTTT
NM_000927.4:c.2685+501_2685+509delinsCTTTCTTTT NP_000918.2:n.2685+501_2685+509delinsCTTTCTTTT
NM_001348944.1:c.2685+501_2685+509delinsCTTTCTTTT NP_001335873.1:n.2685+501_2685+509delinsCTTTCTTTT
NM_001348945.1:c.2895+501_2895+509delinsCTTTCTTTT NP_001335874.1:n.2895+501_2895+509delinsCTTTCTTTT
NM_001348946.1:c.2685+501_2685+509delinsCTTTCTTTT NP_001335875.1:n.2685+501_2685+509delinsCTTTCTTTT
NM_001348946.2:c.2685+501_2685+509delinsCTTTCTTTT MANE Select NP_001335875.1:n.2685+501_2685+509delinsCTTTCTTTT
NM_000927.5:c.2685+501_2685+509delinsCTTTCTTTT NP_000918.2:n.2685+501_2685+509delinsCTTTCTTTT
NM_001348944.2:c.2685+501_2685+509delinsCTTTCTTTT NP_001335873.1:n.2685+501_2685+509delinsCTTTCTTTT
NM_001348945.2:c.2895+501_2895+509delinsCTTTCTTTT NP_001335874.1:n.2895+501_2895+509delinsCTTTCTTTT