Canonical Allele Identifier: CA1427019561

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620593G= , CM000665.2:g.186620593G=	GRCh38
NC_000003.11:g.186338382G= , CM000665.1:g.186338382G=	GRCh37
NC_000003.10:g.187821076G=	NCBI36
NG_011436.1:g.12533G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001622.4:c.767G= MANE Select	NP_001613.2:p.Ser256=
ENST00000411641.7:c.767G= MANE Select	ENSP00000393887.2:p.Ser256=
NM_001354571.1:c.770G=	NP_001341500.1:p.Ser257=
NM_001354571.2:c.770G=	NP_001341500.1:p.Ser257=
NM_001354572.1:c.764G=	NP_001341501.1:p.Ser255=
NM_001354572.2:c.764G=	NP_001341501.1:p.Ser255=
NM_001354573.1:c.683G=	NP_001341502.1:p.Ser228=
NM_001354573.2:c.683G=	NP_001341502.1:p.Ser228=
NM_001622.2:c.767G=	NP_001613.2:p.Ser256=
NM_001622.3:c.767G=	NP_001613.2:p.Ser256=
ENST00000273784.5:c.770G=	ENSP00000273784.5:p.Ser257=
ENST00000411641.6:c.767G=	ENSP00000393887.2:p.Ser256=