Canonical Allele Identifier: CA2668958441

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617967-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617967_186617968insGG , CM000665.2:g.186617967_186617968insGG	GRCh38
NC_000003.11:g.186335756_186335757insGG , CM000665.1:g.186335756_186335757insGG	GRCh37
NC_000003.10:g.187818450_187818451insGG	NCBI36
NG_011436.1:g.9907_9908insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-569_574-568insGG MANE Select	ENSP00000393887.2:n.574-569_574-568insGG
ENST00000273784.5:c.577-569_577-568insGG	ENSP00000273784.5:n.577-569_577-568insGG
ENST00000411641.6:c.574-569_574-568insGG	ENSP00000393887.2:n.574-569_574-568insGG
ENST00000478441.1:n.1247_1248insGG
NM_001622.2:c.574-569_574-568insGG	NP_001613.2:n.574-569_574-568insGG
NM_001354571.1:c.577-569_577-568insGG	NP_001341500.1:n.577-569_577-568insGG
NM_001354572.1:c.571-569_571-568insGG	NP_001341501.1:n.571-569_571-568insGG
NM_001354573.1:c.574-569_574-568insGG	NP_001341502.1:n.574-569_574-568insGG
NM_001622.3:c.574-569_574-568insGG	NP_001613.2:n.574-569_574-568insGG
NM_001622.4:c.574-569_574-568insGG MANE Select	NP_001613.2:n.574-569_574-568insGG
NM_001354571.2:c.577-569_577-568insGG	NP_001341500.1:n.577-569_577-568insGG
NM_001354572.2:c.571-569_571-568insGG	NP_001341501.1:n.571-569_571-568insGG
NM_001354573.2:c.574-569_574-568insGG	NP_001341502.1:n.574-569_574-568insGG