Canonical Allele Identifier: CA1427016151

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186613082T= , CM000665.2:g.186613082T=	GRCh38
NC_000003.11:g.186330871T= , CM000665.1:g.186330871T=	GRCh37
NC_000003.10:g.187813565T=	NCBI36
NG_011436.1:g.5022T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.-60T= MANE Select	ENSP00000393887.2:n.-60T=
ENST00000273784.5:c.-60T=	ENSP00000273784.5:n.-60T=
ENST00000411641.6:c.-60T=	ENSP00000393887.2:n.-60T=
NM_001622.2:c.-60T=	NP_001613.2:n.-60T=
NM_001354571.1:c.-60T=	NP_001341500.1:n.-60T=
NM_001354572.1:c.-60T=	NP_001341501.1:n.-60T=
NM_001354573.1:c.-60T=	NP_001341502.1:n.-60T=
NM_001622.3:c.-60T=	NP_001613.2:n.-60T=
NM_001622.4:c.-60T= MANE Select	NP_001613.2:n.-60T=
NM_001354571.2:c.-60T=	NP_001341500.1:n.-60T=
NM_001354572.2:c.-60T=	NP_001341501.1:n.-60T=
NM_001354573.2:c.-60T=	NP_001341502.1:n.-60T=