Canonical Allele Identifier: CA2668958497

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617972-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617972_186617973insG , CM000665.2:g.186617972_186617973insG	GRCh38
NC_000003.11:g.186335761_186335762insG , CM000665.1:g.186335761_186335762insG	GRCh37
NC_000003.10:g.187818455_187818456insG	NCBI36
NG_011436.1:g.9912_9913insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-564_574-563insG MANE Select	ENSP00000393887.2:n.574-564_574-563insG
ENST00000273784.5:c.577-564_577-563insG	ENSP00000273784.5:n.577-564_577-563insG
ENST00000411641.6:c.574-564_574-563insG	ENSP00000393887.2:n.574-564_574-563insG
ENST00000478441.1:n.1252_1253insG
NM_001622.2:c.574-564_574-563insG	NP_001613.2:n.574-564_574-563insG
NM_001354571.1:c.577-564_577-563insG	NP_001341500.1:n.577-564_577-563insG
NM_001354572.1:c.571-564_571-563insG	NP_001341501.1:n.571-564_571-563insG
NM_001354573.1:c.574-564_574-563insG	NP_001341502.1:n.574-564_574-563insG
NM_001622.3:c.574-564_574-563insG	NP_001613.2:n.574-564_574-563insG
NM_001622.4:c.574-564_574-563insG MANE Select	NP_001613.2:n.574-564_574-563insG
NM_001354571.2:c.577-564_577-563insG	NP_001341500.1:n.577-564_577-563insG
NM_001354572.2:c.571-564_571-563insG	NP_001341501.1:n.571-564_571-563insG
NM_001354573.2:c.574-564_574-563insG	NP_001341502.1:n.574-564_574-563insG