Canonical Allele Identifier: CA1723626157

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515291A= , CM000669.2:g.87515291A=	GRCh38
NC_000007.13:g.87144607A= , CM000669.1:g.87144607A=	GRCh37
NC_000007.12:g.86982543A=	NCBI36
NG_011513.1:g.202958T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3222T=	ENSP00000265724.3:p.Cys1074=
ENST00000622132.5:c.3222T= MANE Select	ENSP00000478255.1:p.Cys1074=
ENST00000265724.7:c.3222T=	ENSP00000265724.3:p.Cys1074=
ENST00000475929.5:n.378T=
ENST00000488737.6:n.864T=
ENST00000496821.5:n.850T=
ENST00000543898.5:c.3030T=	ENSP00000444095.1:p.Cys1010=
ENST00000622132.4:c.3222T=	ENSP00000478255.1:p.Cys1074=
NM_000927.4:c.3222T=	NP_000918.2:p.Cys1074=
NM_001348944.1:c.3222T=	NP_001335873.1:p.Cys1074=
NM_001348945.1:c.3432T=	NP_001335874.1:p.Cys1144=
NM_001348946.1:c.3222T=	NP_001335875.1:p.Cys1074=
NM_001348946.2:c.3222T= MANE Select	NP_001335875.1:p.Cys1074=
NM_000927.5:c.3222T=	NP_000918.2:p.Cys1074=
NM_001348944.2:c.3222T=	NP_001335873.1:p.Cys1074=
NM_001348945.2:c.3432T=	NP_001335874.1:p.Cys1144=