Canonical Allele Identifier: CA2668959071

Gene: AHSG

Linked Data

• gnomAD v4: 3-186618746-C-CAAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618747_186618750dup , CM000665.2:g.186618747_186618750dup	GRCh38
NC_000003.11:g.186336536_186336539dup , CM000665.1:g.186336536_186336539dup	GRCh37
NC_000003.10:g.187819230_187819233dup	NCBI36
NG_011436.1:g.10687_10690dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.675+110_675+113dup MANE Select	ENSP00000393887.2:n.675+110_675+113dup
ENST00000273784.5:c.678+110_678+113dup	ENSP00000273784.5:n.678+110_678+113dup
ENST00000411641.6:c.675+110_675+113dup	ENSP00000393887.2:n.675+110_675+113dup
NM_001622.2:c.675+110_675+113dup	NP_001613.2:n.675+110_675+113dup
NM_001354571.1:c.678+110_678+113dup	NP_001341500.1:n.678+110_678+113dup
NM_001354572.1:c.672+110_672+113dup	NP_001341501.1:n.672+110_672+113dup
NM_001354573.1:c.675+110_675+113dup	NP_001341502.1:n.675+110_675+113dup
NM_001622.3:c.675+110_675+113dup	NP_001613.2:n.675+110_675+113dup
NM_001622.4:c.675+110_675+113dup MANE Select	NP_001613.2:n.675+110_675+113dup
NM_001354571.2:c.678+110_678+113dup	NP_001341500.1:n.678+110_678+113dup
NM_001354572.2:c.672+110_672+113dup	NP_001341501.1:n.672+110_672+113dup
NM_001354573.2:c.675+110_675+113dup	NP_001341502.1:n.675+110_675+113dup