Canonical Allele Identifier: CA1723626145

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515271T= , CM000669.2:g.87515271T=	GRCh38
NC_000007.13:g.87144587T= , CM000669.1:g.87144587T=	GRCh37
NC_000007.12:g.86982523T=	NCBI36
NG_011513.1:g.202978A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3242A=	ENSP00000265724.3:p.Gln1081=
ENST00000622132.5:c.3242A= MANE Select	ENSP00000478255.1:p.Gln1081=
ENST00000265724.7:c.3242A=	ENSP00000265724.3:p.Gln1081=
ENST00000475929.5:n.398A=
ENST00000488737.6:n.884A=
ENST00000496821.5:n.870A=
ENST00000543898.5:c.3050A=	ENSP00000444095.1:p.Gln1017=
ENST00000622132.4:c.3242A=	ENSP00000478255.1:p.Gln1081=
NM_000927.4:c.3242A=	NP_000918.2:p.Gln1081=
NM_001348944.1:c.3242A=	NP_001335873.1:p.Gln1081=
NM_001348945.1:c.3452A=	NP_001335874.1:p.Gln1151=
NM_001348946.1:c.3242A=	NP_001335875.1:p.Gln1081=
NM_001348946.2:c.3242A= MANE Select	NP_001335875.1:p.Gln1081=
NM_000927.5:c.3242A=	NP_000918.2:p.Gln1081=
NM_001348944.2:c.3242A=	NP_001335873.1:p.Gln1081=
NM_001348945.2:c.3452A=	NP_001335874.1:p.Gln1151=