Canonical Allele Identifier: CA2542559903

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617970-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617970_186617971insAT , CM000665.2:g.186617970_186617971insAT	GRCh38
NC_000003.11:g.186335759_186335760insAT , CM000665.1:g.186335759_186335760insAT	GRCh37
NC_000003.10:g.187818453_187818454insAT	NCBI36
NG_011436.1:g.9910_9911insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-566_574-565insAT MANE Select	ENSP00000393887.2:n.574-566_574-565insAT
ENST00000273784.5:c.577-566_577-565insAT	ENSP00000273784.5:n.577-566_577-565insAT
ENST00000411641.6:c.574-566_574-565insAT	ENSP00000393887.2:n.574-566_574-565insAT
ENST00000478441.1:n.1250_1251insAT
NM_001622.2:c.574-566_574-565insAT	NP_001613.2:n.574-566_574-565insAT
NM_001354571.1:c.577-566_577-565insAT	NP_001341500.1:n.577-566_577-565insAT
NM_001354572.1:c.571-566_571-565insAT	NP_001341501.1:n.571-566_571-565insAT
NM_001354573.1:c.574-566_574-565insAT	NP_001341502.1:n.574-566_574-565insAT
NM_001622.3:c.574-566_574-565insAT	NP_001613.2:n.574-566_574-565insAT
NM_001622.4:c.574-566_574-565insAT MANE Select	NP_001613.2:n.574-566_574-565insAT
NM_001354571.2:c.577-566_577-565insAT	NP_001341500.1:n.577-566_577-565insAT
NM_001354572.2:c.571-566_571-565insAT	NP_001341501.1:n.571-566_571-565insAT
NM_001354573.2:c.574-566_574-565insAT	NP_001341502.1:n.574-566_574-565insAT