Canonical Allele Identifier: CA1427019588

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620655G= , CM000665.2:g.186620655G=	GRCh38
NC_000003.11:g.186338444G= , CM000665.1:g.186338444G=	GRCh37
NC_000003.10:g.187821138G=	NCBI36
NG_011436.1:g.12595G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.829G= MANE Select	ENSP00000393887.2:p.Ala277=
ENST00000273784.5:c.832G=	ENSP00000273784.5:p.Ala278=
ENST00000411641.6:c.829G=	ENSP00000393887.2:p.Ala277=
NM_001622.2:c.829G=	NP_001613.2:p.Ala277=
NM_001354571.1:c.832G=	NP_001341500.1:p.Ala278=
NM_001354572.1:c.826G=	NP_001341501.1:p.Ala276=
NM_001354573.1:c.745G=	NP_001341502.1:p.Ala249=
NM_001622.3:c.829G=	NP_001613.2:p.Ala277=
NM_001622.4:c.829G= MANE Select	NP_001613.2:p.Ala277=
NM_001354571.2:c.832G=	NP_001341500.1:p.Ala278=
NM_001354572.2:c.826G=	NP_001341501.1:p.Ala276=
NM_001354573.2:c.745G=	NP_001341502.1:p.Ala249=