Canonical Allele Identifier: CA1723631431

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530862_87530873delinsAAAGAAAGAAAG , CM000669.2:g.87530862_87530873delinsAAAGAAAGAAAG	GRCh38
NC_000007.13:g.87160178_87160189delinsAAAGAAAGAAAG , CM000669.1:g.87160178_87160189delinsAAAGAAAGAAAG	GRCh37
NC_000007.12:g.86998114_86998125delinsAAAGAAAGAAAG	NCBI36
NG_011513.1:g.187376_187387delinsCTTTCTTTCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+421_2685+432delinsCTTTCTTTCTTT	ENSP00000265724.3:n.2685+421_2685+432delinsCTTTCTTTCTTT
ENST00000622132.5:c.2685+421_2685+432delinsCTTTCTTTCTTT MANE Select	ENSP00000478255.1:n.2685+421_2685+432delinsCTTTCTTTCTTT
ENST00000265724.7:c.2685+421_2685+432delinsCTTTCTTTCTTT	ENSP00000265724.3:n.2685+421_2685+432delinsCTTTCTTTCTTT
ENST00000488737.6:n.327+421_327+432delinsCTTTCTTTCTTT
ENST00000496821.5:n.313+421_313+432delinsCTTTCTTTCTTT
ENST00000543898.5:c.2493+421_2493+432delinsCTTTCTTTCTTT	ENSP00000444095.1:n.2493+421_2493+432delinsCTTTCTTTCTTT
ENST00000622132.4:c.2685+421_2685+432delinsCTTTCTTTCTTT	ENSP00000478255.1:n.2685+421_2685+432delinsCTTTCTTTCTTT
NM_000927.4:c.2685+421_2685+432delinsCTTTCTTTCTTT	NP_000918.2:n.2685+421_2685+432delinsCTTTCTTTCTTT
NM_001348944.1:c.2685+421_2685+432delinsCTTTCTTTCTTT	NP_001335873.1:n.2685+421_2685+432delinsCTTTCTTTCTTT
NM_001348945.1:c.2895+421_2895+432delinsCTTTCTTTCTTT	NP_001335874.1:n.2895+421_2895+432delinsCTTTCTTTCTTT
NM_001348946.1:c.2685+421_2685+432delinsCTTTCTTTCTTT	NP_001335875.1:n.2685+421_2685+432delinsCTTTCTTTCTTT
NM_001348946.2:c.2685+421_2685+432delinsCTTTCTTTCTTT MANE Select	NP_001335875.1:n.2685+421_2685+432delinsCTTTCTTTCTTT
NM_000927.5:c.2685+421_2685+432delinsCTTTCTTTCTTT	NP_000918.2:n.2685+421_2685+432delinsCTTTCTTTCTTT
NM_001348944.2:c.2685+421_2685+432delinsCTTTCTTTCTTT	NP_001335873.1:n.2685+421_2685+432delinsCTTTCTTTCTTT
NM_001348945.2:c.2895+421_2895+432delinsCTTTCTTTCTTT	NP_001335874.1:n.2895+421_2895+432delinsCTTTCTTTCTTT