Canonical Allele Identifier: CA1427018714

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618576G= , CM000665.2:g.186618576G=	GRCh38
NC_000003.11:g.186336365G= , CM000665.1:g.186336365G=	GRCh37
NC_000003.10:g.187819059G=	NCBI36
NG_011436.1:g.10516G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.614G= MANE Select	ENSP00000393887.2:p.Gly205=
ENST00000273784.5:c.617G=	ENSP00000273784.5:p.Gly206=
ENST00000411641.6:c.614G=	ENSP00000393887.2:p.Gly205=
NM_001622.2:c.614G=	NP_001613.2:p.Gly205=
NM_001354571.1:c.617G=	NP_001341500.1:p.Gly206=
NM_001354572.1:c.611G=	NP_001341501.1:p.Gly204=
NM_001354573.1:c.614G=	NP_001341502.1:p.Gly205=
NM_001622.3:c.614G=	NP_001613.2:p.Gly205=
NM_001622.4:c.614G= MANE Select	NP_001613.2:p.Gly205=
NM_001354571.2:c.617G=	NP_001341500.1:p.Gly206=
NM_001354572.2:c.611G=	NP_001341501.1:p.Gly204=
NM_001354573.2:c.614G=	NP_001341502.1:p.Gly205=