Canonical Allele Identifier: CA1427018733

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618624T= , CM000665.2:g.186618624T=	GRCh38
NC_000003.11:g.186336413T= , CM000665.1:g.186336413T=	GRCh37
NC_000003.10:g.187819107T=	NCBI36
NG_011436.1:g.10564T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.662T= MANE Select	ENSP00000393887.2:p.Leu221=
ENST00000273784.5:c.665T=	ENSP00000273784.5:p.Leu222=
ENST00000411641.6:c.662T=	ENSP00000393887.2:p.Leu221=
NM_001622.2:c.662T=	NP_001613.2:p.Leu221=
NM_001354571.1:c.665T=	NP_001341500.1:p.Leu222=
NM_001354572.1:c.659T=	NP_001341501.1:p.Leu220=
NM_001354573.1:c.662T=	NP_001341502.1:p.Leu221=
NM_001622.3:c.662T=	NP_001613.2:p.Leu221=
NM_001622.4:c.662T= MANE Select	NP_001613.2:p.Leu221=
NM_001354571.2:c.665T=	NP_001341500.1:p.Leu222=
NM_001354572.2:c.659T=	NP_001341501.1:p.Leu220=
NM_001354573.2:c.662T=	NP_001341502.1:p.Leu221=