Canonical Allele Identifier: CA1427018473

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618035_186618036delinsCT , CM000665.2:g.186618035_186618036delinsCT	GRCh38
NC_000003.11:g.186335824_186335825delinsCT , CM000665.1:g.186335824_186335825delinsCT	GRCh37
NC_000003.10:g.187818518_187818519delinsCT	NCBI36
NG_011436.1:g.9975_9976delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-501_574-500delinsCT MANE Select	ENSP00000393887.2:n.574-501_574-500delinsCT
ENST00000273784.5:c.577-501_577-500delinsCT	ENSP00000273784.5:n.577-501_577-500delinsCT
ENST00000411641.6:c.574-501_574-500delinsCT	ENSP00000393887.2:n.574-501_574-500delinsCT
NM_001622.2:c.574-501_574-500delinsCT	NP_001613.2:n.574-501_574-500delinsCT
NM_001354571.1:c.577-501_577-500delinsCT	NP_001341500.1:n.577-501_577-500delinsCT
NM_001354572.1:c.571-501_571-500delinsCT	NP_001341501.1:n.571-501_571-500delinsCT
NM_001354573.1:c.574-501_574-500delinsCT	NP_001341502.1:n.574-501_574-500delinsCT
NM_001622.3:c.574-501_574-500delinsCT	NP_001613.2:n.574-501_574-500delinsCT
NM_001622.4:c.574-501_574-500delinsCT MANE Select	NP_001613.2:n.574-501_574-500delinsCT
NM_001354571.2:c.577-501_577-500delinsCT	NP_001341500.1:n.577-501_577-500delinsCT
NM_001354572.2:c.571-501_571-500delinsCT	NP_001341501.1:n.571-501_571-500delinsCT
NM_001354573.2:c.574-501_574-500delinsCT	NP_001341502.1:n.574-501_574-500delinsCT