Canonical Allele Identifier: CA2668958580

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617988-A-AAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617988_186617989insAAT , CM000665.2:g.186617988_186617989insAAT	GRCh38
NC_000003.11:g.186335777_186335778insAAT , CM000665.1:g.186335777_186335778insAAT	GRCh37
NC_000003.10:g.187818471_187818472insAAT	NCBI36
NG_011436.1:g.9928_9929insAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-548_574-547insAAT MANE Select	ENSP00000393887.2:n.574-548_574-547insAAT
ENST00000273784.5:c.577-548_577-547insAAT	ENSP00000273784.5:n.577-548_577-547insAAT
ENST00000411641.6:c.574-548_574-547insAAT	ENSP00000393887.2:n.574-548_574-547insAAT
ENST00000478441.1:n.1268_1269insAAT
NM_001622.2:c.574-548_574-547insAAT	NP_001613.2:n.574-548_574-547insAAT
NM_001354571.1:c.577-548_577-547insAAT	NP_001341500.1:n.577-548_577-547insAAT
NM_001354572.1:c.571-548_571-547insAAT	NP_001341501.1:n.571-548_571-547insAAT
NM_001354573.1:c.574-548_574-547insAAT	NP_001341502.1:n.574-548_574-547insAAT
NM_001622.3:c.574-548_574-547insAAT	NP_001613.2:n.574-548_574-547insAAT
NM_001622.4:c.574-548_574-547insAAT MANE Select	NP_001613.2:n.574-548_574-547insAAT
NM_001354571.2:c.577-548_577-547insAAT	NP_001341500.1:n.577-548_577-547insAAT
NM_001354572.2:c.571-548_571-547insAAT	NP_001341501.1:n.571-548_571-547insAAT
NM_001354573.2:c.574-548_574-547insAAT	NP_001341502.1:n.574-548_574-547insAAT