Canonical Allele Identifier: CA1427016917

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186614792G= , CM000665.2:g.186614792G=	GRCh38
NC_000003.11:g.186332581G= , CM000665.1:g.186332581G=	GRCh37
NC_000003.10:g.187815275G=	NCBI36
NG_011436.1:g.6732G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.214-893G= MANE Select	ENSP00000393887.2:n.214-893G=
ENST00000273784.5:c.214-893G=	ENSP00000273784.5:n.214-893G=
ENST00000411641.6:c.214-893G=	ENSP00000393887.2:n.214-893G=
ENST00000478441.1:n.271-893G=
NM_001622.2:c.214-893G=	NP_001613.2:n.214-893G=
NM_001354571.1:c.214-893G=	NP_001341500.1:n.214-893G=
NM_001354572.1:c.214-896G=	NP_001341501.1:n.214-896G=
NM_001354573.1:c.214-893G=	NP_001341502.1:n.214-893G=
NM_001622.3:c.214-893G=	NP_001613.2:n.214-893G=
NM_001622.4:c.214-893G= MANE Select	NP_001613.2:n.214-893G=
NM_001354571.2:c.214-893G=	NP_001341500.1:n.214-893G=
NM_001354572.2:c.214-896G=	NP_001341501.1:n.214-896G=
NM_001354573.2:c.214-893G=	NP_001341502.1:n.214-893G=