Canonical Allele Identifier: CA1723621353

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87504002A= , CM000669.2:g.87504002A=	GRCh38
NC_000007.13:g.87133318A= , CM000669.1:g.87133318A=	GRCh37
NC_000007.12:g.86971254A=	NCBI36
NG_011513.1:g.214247T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.*241T=	ENSP00000265724.3:n.*241T=
ENST00000622132.5:c.*241T= MANE Select	ENSP00000478255.1:n.*241T=
ENST00000265724.7:c.*241T=	ENSP00000265724.3:n.*241T=
ENST00000488737.6:n.1726T=
ENST00000543898.5:c.*241T=	ENSP00000444095.1:n.*241T=
ENST00000622132.4:c.*241T=	ENSP00000478255.1:n.*241T=
NM_000927.4:c.*241T=	NP_000918.2:n.*241T=
NM_001348944.1:c.*241T=	NP_001335873.1:n.*241T=
NM_001348945.1:c.*241T=	NP_001335874.1:n.*241T=
NM_001348946.1:c.*241T=	NP_001335875.1:n.*241T=
NM_001348946.2:c.*241T= MANE Select	NP_001335875.1:n.*241T=
NM_000927.5:c.*241T=	NP_000918.2:n.*241T=
NM_001348944.2:c.*241T=	NP_001335873.1:n.*241T=
NM_001348945.2:c.*241T=	NP_001335874.1:n.*241T=