Canonical Allele Identifier: CA1723626139

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515259C= , CM000669.2:g.87515259C=	GRCh38
NC_000007.13:g.87144575C= , CM000669.1:g.87144575C=	GRCh37
NC_000007.12:g.86982511C=	NCBI36
NG_011513.1:g.202990G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3254G=	ENSP00000265724.3:p.Arg1085=
ENST00000622132.5:c.3254G= MANE Select	ENSP00000478255.1:p.Arg1085=
ENST00000265724.7:c.3254G=	ENSP00000265724.3:p.Arg1085=
ENST00000475929.5:n.410G=
ENST00000488737.6:n.896G=
ENST00000496821.5:n.882G=
ENST00000543898.5:c.3062G=	ENSP00000444095.1:p.Arg1021=
ENST00000622132.4:c.3254G=	ENSP00000478255.1:p.Arg1085=
NM_000927.4:c.3254G=	NP_000918.2:p.Arg1085=
NM_001348944.1:c.3254G=	NP_001335873.1:p.Arg1085=
NM_001348945.1:c.3464G=	NP_001335874.1:p.Arg1155=
NM_001348946.1:c.3254G=	NP_001335875.1:p.Arg1085=
NM_001348946.2:c.3254G= MANE Select	NP_001335875.1:p.Arg1085=
NM_000927.5:c.3254G=	NP_000918.2:p.Arg1085=
NM_001348944.2:c.3254G=	NP_001335873.1:p.Arg1085=
NM_001348945.2:c.3464G=	NP_001335874.1:p.Arg1155=