Canonical Allele Identifier: CA1427019267

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186619924T= , CM000665.2:g.186619924T=	GRCh38
NC_000003.11:g.186337713T= , CM000665.1:g.186337713T=	GRCh37
NC_000003.10:g.187820407T=	NCBI36
NG_011436.1:g.11864T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001622.4:c.743T= MANE Select	NP_001613.2:p.Met248=
ENST00000411641.7:c.743T= MANE Select	ENSP00000393887.2:p.Met248=
NM_001354571.1:c.746T=	NP_001341500.1:p.Met249=
NM_001354571.2:c.746T=	NP_001341500.1:p.Met249=
NM_001354572.1:c.740T=	NP_001341501.1:p.Met247=
NM_001354572.2:c.740T=	NP_001341501.1:p.Met247=
NM_001354573.1:c.676-662T=	NP_001341502.1:n.676-662T=
NM_001354573.2:c.676-662T=	NP_001341502.1:n.676-662T=
NM_001622.2:c.743T=	NP_001613.2:p.Met248=
NM_001622.3:c.743T=	NP_001613.2:p.Met248=
ENST00000273784.5:c.746T=	ENSP00000273784.5:p.Met249=
ENST00000411641.6:c.743T=	ENSP00000393887.2:p.Met248=