Canonical Allele Identifier: CA2668958533

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617977-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617977_186617978insG , CM000665.2:g.186617977_186617978insG	GRCh38
NC_000003.11:g.186335766_186335767insG , CM000665.1:g.186335766_186335767insG	GRCh37
NC_000003.10:g.187818460_187818461insG	NCBI36
NG_011436.1:g.9917_9918insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-559_574-558insG MANE Select	ENSP00000393887.2:n.574-559_574-558insG
ENST00000273784.5:c.577-559_577-558insG	ENSP00000273784.5:n.577-559_577-558insG
ENST00000411641.6:c.574-559_574-558insG	ENSP00000393887.2:n.574-559_574-558insG
ENST00000478441.1:n.1257_1258insG
NM_001622.2:c.574-559_574-558insG	NP_001613.2:n.574-559_574-558insG
NM_001354571.1:c.577-559_577-558insG	NP_001341500.1:n.577-559_577-558insG
NM_001354572.1:c.571-559_571-558insG	NP_001341501.1:n.571-559_571-558insG
NM_001354573.1:c.574-559_574-558insG	NP_001341502.1:n.574-559_574-558insG
NM_001622.3:c.574-559_574-558insG	NP_001613.2:n.574-559_574-558insG
NM_001622.4:c.574-559_574-558insG MANE Select	NP_001613.2:n.574-559_574-558insG
NM_001354571.2:c.577-559_577-558insG	NP_001341500.1:n.577-559_577-558insG
NM_001354572.2:c.571-559_571-558insG	NP_001341501.1:n.571-559_571-558insG
NM_001354573.2:c.574-559_574-558insG	NP_001341502.1:n.574-559_574-558insG