Canonical Allele Identifier: CA1723621336

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503951A= , CM000669.2:g.87503951A=	GRCh38
NC_000007.13:g.87133267A= , CM000669.1:g.87133267A=	GRCh37
NC_000007.12:g.86971203A=	NCBI36
NG_011513.1:g.214298T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.*292T=	ENSP00000265724.3:n.*292T=
ENST00000622132.5:c.*292T= MANE Select	ENSP00000478255.1:n.*292T=
ENST00000265724.7:c.*292T=	ENSP00000265724.3:n.*292T=
ENST00000488737.6:n.1777T=
ENST00000543898.5:c.*292T=	ENSP00000444095.1:n.*292T=
ENST00000622132.4:c.*292T=	ENSP00000478255.1:n.*292T=
NM_000927.4:c.*292T=	NP_000918.2:n.*292T=
NM_001348944.1:c.*292T=	NP_001335873.1:n.*292T=
NM_001348945.1:c.*292T=	NP_001335874.1:n.*292T=
NM_001348946.1:c.*292T=	NP_001335875.1:n.*292T=
NM_001348946.2:c.*292T= MANE Select	NP_001335875.1:n.*292T=
NM_000927.5:c.*292T=	NP_000918.2:n.*292T=
NM_001348944.2:c.*292T=	NP_001335873.1:n.*292T=
NM_001348945.2:c.*292T=	NP_001335874.1:n.*292T=