Canonical Allele Identifier: CA1723631447

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530863_87530873delinsAAGAAAGAAAG , CM000669.2:g.87530863_87530873delinsAAGAAAGAAAG	GRCh38
NC_000007.13:g.87160179_87160189delinsAAGAAAGAAAG , CM000669.1:g.87160179_87160189delinsAAGAAAGAAAG	GRCh37
NC_000007.12:g.86998115_86998125delinsAAGAAAGAAAG	NCBI36
NG_011513.1:g.187376_187386delinsCTTTCTTTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+421_2685+431delinsCTTTCTTTCTT	ENSP00000265724.3:n.2685+421_2685+431delinsCTTTCTTTCTT
ENST00000622132.5:c.2685+421_2685+431delinsCTTTCTTTCTT MANE Select	ENSP00000478255.1:n.2685+421_2685+431delinsCTTTCTTTCTT
ENST00000265724.7:c.2685+421_2685+431delinsCTTTCTTTCTT	ENSP00000265724.3:n.2685+421_2685+431delinsCTTTCTTTCTT
ENST00000488737.6:n.327+421_327+431delinsCTTTCTTTCTT
ENST00000496821.5:n.313+421_313+431delinsCTTTCTTTCTT
ENST00000543898.5:c.2493+421_2493+431delinsCTTTCTTTCTT	ENSP00000444095.1:n.2493+421_2493+431delinsCTTTCTTTCTT
ENST00000622132.4:c.2685+421_2685+431delinsCTTTCTTTCTT	ENSP00000478255.1:n.2685+421_2685+431delinsCTTTCTTTCTT
NM_000927.4:c.2685+421_2685+431delinsCTTTCTTTCTT	NP_000918.2:n.2685+421_2685+431delinsCTTTCTTTCTT
NM_001348944.1:c.2685+421_2685+431delinsCTTTCTTTCTT	NP_001335873.1:n.2685+421_2685+431delinsCTTTCTTTCTT
NM_001348945.1:c.2895+421_2895+431delinsCTTTCTTTCTT	NP_001335874.1:n.2895+421_2895+431delinsCTTTCTTTCTT
NM_001348946.1:c.2685+421_2685+431delinsCTTTCTTTCTT	NP_001335875.1:n.2685+421_2685+431delinsCTTTCTTTCTT
NM_001348946.2:c.2685+421_2685+431delinsCTTTCTTTCTT MANE Select	NP_001335875.1:n.2685+421_2685+431delinsCTTTCTTTCTT
NM_000927.5:c.2685+421_2685+431delinsCTTTCTTTCTT	NP_000918.2:n.2685+421_2685+431delinsCTTTCTTTCTT
NM_001348944.2:c.2685+421_2685+431delinsCTTTCTTTCTT	NP_001335873.1:n.2685+421_2685+431delinsCTTTCTTTCTT
NM_001348945.2:c.2895+421_2895+431delinsCTTTCTTTCTT	NP_001335874.1:n.2895+421_2895+431delinsCTTTCTTTCTT