Canonical Allele Identifier: CA1723631094
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530818_87530830delinsAAAGCAAGAAAGC , CM000669.2:g.87530818_87530830delinsAAAGCAAGAAAGC GRCh38
NC_000007.13:g.87160134_87160146delinsAAAGCAAGAAAGC , CM000669.1:g.87160134_87160146delinsAAAGCAAGAAAGC GRCh37
NC_000007.12:g.86998070_86998082delinsAAAGCAAGAAAGC NCBI36
NG_011513.1:g.187419_187431delinsGCTTTCTTGCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+464_2685+476delinsGCTTTCTTGCTTT ENSP00000265724.3:n.2685+464_2685+476delinsGCTTTCTTGCTTT
ENST00000622132.5:c.2685+464_2685+476delinsGCTTTCTTGCTTT MANE Select ENSP00000478255.1:n.2685+464_2685+476delinsGCTTTCTTGCTTT
ENST00000265724.7:c.2685+464_2685+476delinsGCTTTCTTGCTTT ENSP00000265724.3:n.2685+464_2685+476delinsGCTTTCTTGCTTT
ENST00000488737.6:n.327+464_327+476delinsGCTTTCTTGCTTT
ENST00000496821.5:n.313+464_313+476delinsGCTTTCTTGCTTT
ENST00000543898.5:c.2493+464_2493+476delinsGCTTTCTTGCTTT ENSP00000444095.1:n.2493+464_2493+476delinsGCTTTCTTGCTTT
ENST00000622132.4:c.2685+464_2685+476delinsGCTTTCTTGCTTT ENSP00000478255.1:n.2685+464_2685+476delinsGCTTTCTTGCTTT
NM_000927.4:c.2685+464_2685+476delinsGCTTTCTTGCTTT NP_000918.2:n.2685+464_2685+476delinsGCTTTCTTGCTTT
NM_001348944.1:c.2685+464_2685+476delinsGCTTTCTTGCTTT NP_001335873.1:n.2685+464_2685+476delinsGCTTTCTTGCTTT
NM_001348945.1:c.2895+464_2895+476delinsGCTTTCTTGCTTT NP_001335874.1:n.2895+464_2895+476delinsGCTTTCTTGCTTT
NM_001348946.1:c.2685+464_2685+476delinsGCTTTCTTGCTTT NP_001335875.1:n.2685+464_2685+476delinsGCTTTCTTGCTTT
NM_001348946.2:c.2685+464_2685+476delinsGCTTTCTTGCTTT MANE Select NP_001335875.1:n.2685+464_2685+476delinsGCTTTCTTGCTTT
NM_000927.5:c.2685+464_2685+476delinsGCTTTCTTGCTTT NP_000918.2:n.2685+464_2685+476delinsGCTTTCTTGCTTT
NM_001348944.2:c.2685+464_2685+476delinsGCTTTCTTGCTTT NP_001335873.1:n.2685+464_2685+476delinsGCTTTCTTGCTTT
NM_001348945.2:c.2895+464_2895+476delinsGCTTTCTTGCTTT NP_001335874.1:n.2895+464_2895+476delinsGCTTTCTTGCTTT