Canonical Allele Identifier: CA1723623771

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87509442A= , CM000669.2:g.87509442A=	GRCh38
NC_000007.13:g.87138758A= , CM000669.1:g.87138758A=	GRCh37
NC_000007.12:g.86976694A=	NCBI36
NG_011513.1:g.208807T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001348946.2:c.3322T= MANE Select	NP_001335875.1:p.Trp1108=
ENST00000622132.5:c.3322T= MANE Select	ENSP00000478255.1:p.Trp1108=
NM_000927.4:c.3322T=	NP_000918.2:p.Trp1108=
NM_000927.5:c.3322T=	NP_000918.2:p.Trp1108=
NM_001348944.1:c.3322T=	NP_001335873.1:p.Trp1108=
NM_001348944.2:c.3322T=	NP_001335873.1:p.Trp1108=
NM_001348945.1:c.3532T=	NP_001335874.1:p.Trp1178=
NM_001348945.2:c.3532T=	NP_001335874.1:p.Trp1178=
NM_001348946.1:c.3322T=	NP_001335875.1:p.Trp1108=
ENST00000265724.7:c.3322T=	ENSP00000265724.3:p.Trp1108=
ENST00000265724.8:c.3322T=	ENSP00000265724.3:p.Trp1108=
ENST00000475929.5:n.478T=
ENST00000488737.6:n.964T=
ENST00000543898.5:c.3130T=	ENSP00000444095.1:p.Trp1044=
ENST00000622132.4:c.3322T=	ENSP00000478255.1:p.Trp1108=