Canonical Allele Identifier: CA1723658199

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87583947T= , CM000669.2:g.87583947T=	GRCh38
NC_000007.13:g.87213263T= , CM000669.1:g.87213263T=	GRCh37
NC_000007.12:g.87051199T=	NCBI36
NG_011513.1:g.134302A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.286+1565A=	ENSP00000265724.3:n.286+1565A=
ENST00000622132.5:c.286+1565A= MANE Select	ENSP00000478255.1:n.286+1565A=
ENST00000265724.7:c.286+1565A=	ENSP00000265724.3:n.286+1565A=
ENST00000543898.5:c.286+1565A=	ENSP00000444095.1:n.286+1565A=
ENST00000622132.4:c.286+1565A=	ENSP00000478255.1:n.286+1565A=
NM_000927.4:c.286+1565A=	NP_000918.2:n.286+1565A=
NM_001348944.1:c.286+1565A=	NP_001335873.1:n.286+1565A=
NM_001348945.1:c.496+1565A=	NP_001335874.1:n.496+1565A=
NM_001348946.1:c.286+1565A=	NP_001335875.1:n.286+1565A=
NM_001348946.2:c.286+1565A= MANE Select	NP_001335875.1:n.286+1565A=
NM_000927.5:c.286+1565A=	NP_000918.2:n.286+1565A=
NM_001348944.2:c.286+1565A=	NP_001335873.1:n.286+1565A=
NM_001348945.2:c.496+1565A=	NP_001335874.1:n.496+1565A=