Canonical Allele Identifier: CA1427018709

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618557G= , CM000665.2:g.186618557G=	GRCh38
NC_000003.11:g.186336346G= , CM000665.1:g.186336346G=	GRCh37
NC_000003.10:g.187819040G=	NCBI36
NG_011436.1:g.10497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.595G= MANE Select	ENSP00000393887.2:p.Val199=
ENST00000273784.5:c.598G=	ENSP00000273784.5:p.Val200=
ENST00000411641.6:c.595G=	ENSP00000393887.2:p.Val199=
NM_001622.2:c.595G=	NP_001613.2:p.Val199=
NM_001354571.1:c.598G=	NP_001341500.1:p.Val200=
NM_001354572.1:c.592G=	NP_001341501.1:p.Val198=
NM_001354573.1:c.595G=	NP_001341502.1:p.Val199=
NM_001622.3:c.595G=	NP_001613.2:p.Val199=
NM_001622.4:c.595G= MANE Select	NP_001613.2:p.Val199=
NM_001354571.2:c.598G=	NP_001341500.1:p.Val200=
NM_001354572.2:c.592G=	NP_001341501.1:p.Val198=
NM_001354573.2:c.595G=	NP_001341502.1:p.Val199=