Canonical Allele Identifier: CA1723631226

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530836_87530838delinsAGC , CM000669.2:g.87530836_87530838delinsAGC	GRCh38
NC_000007.13:g.87160152_87160154delinsAGC , CM000669.1:g.87160152_87160154delinsAGC	GRCh37
NC_000007.12:g.86998088_86998090delinsAGC	NCBI36
NG_011513.1:g.187411_187413delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+456_2685+458delinsGCT	ENSP00000265724.3:n.2685+456_2685+458delinsGCT
ENST00000622132.5:c.2685+456_2685+458delinsGCT MANE Select	ENSP00000478255.1:n.2685+456_2685+458delinsGCT
ENST00000265724.7:c.2685+456_2685+458delinsGCT	ENSP00000265724.3:n.2685+456_2685+458delinsGCT
ENST00000488737.6:n.327+456_327+458delinsGCT
ENST00000496821.5:n.313+456_313+458delinsGCT
ENST00000543898.5:c.2493+456_2493+458delinsGCT	ENSP00000444095.1:n.2493+456_2493+458delinsGCT
ENST00000622132.4:c.2685+456_2685+458delinsGCT	ENSP00000478255.1:n.2685+456_2685+458delinsGCT
NM_000927.4:c.2685+456_2685+458delinsGCT	NP_000918.2:n.2685+456_2685+458delinsGCT
NM_001348944.1:c.2685+456_2685+458delinsGCT	NP_001335873.1:n.2685+456_2685+458delinsGCT
NM_001348945.1:c.2895+456_2895+458delinsGCT	NP_001335874.1:n.2895+456_2895+458delinsGCT
NM_001348946.1:c.2685+456_2685+458delinsGCT	NP_001335875.1:n.2685+456_2685+458delinsGCT
NM_001348946.2:c.2685+456_2685+458delinsGCT MANE Select	NP_001335875.1:n.2685+456_2685+458delinsGCT
NM_000927.5:c.2685+456_2685+458delinsGCT	NP_000918.2:n.2685+456_2685+458delinsGCT
NM_001348944.2:c.2685+456_2685+458delinsGCT	NP_001335873.1:n.2685+456_2685+458delinsGCT
NM_001348945.2:c.2895+456_2895+458delinsGCT	NP_001335874.1:n.2895+456_2895+458delinsGCT