Canonical Allele Identifier: CA2668956799

Gene: AHSG

Linked Data

• gnomAD v4: 3-186620574-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620576del , CM000665.2:g.186620576del	GRCh38
NC_000003.11:g.186338365del , CM000665.1:g.186338365del	GRCh37
NC_000003.10:g.187821059del	NCBI36
NG_011436.1:g.12516del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.760-10del MANE Select	ENSP00000393887.2:n.760-10del
ENST00000273784.5:c.763-10del	ENSP00000273784.5:n.763-10del
ENST00000411641.6:c.760-10del	ENSP00000393887.2:n.760-10del
NM_001622.2:c.760-10del	NP_001613.2:n.760-10del
NM_001354571.1:c.763-10del	NP_001341500.1:n.763-10del
NM_001354572.1:c.757-10del	NP_001341501.1:n.757-10del
NM_001354573.1:c.676-10del	NP_001341502.1:n.676-10del
NM_001622.3:c.760-10del	NP_001613.2:n.760-10del
NM_001622.4:c.760-10del MANE Select	NP_001613.2:n.760-10del
NM_001354571.2:c.763-10del	NP_001341500.1:n.763-10del
NM_001354572.2:c.757-10del	NP_001341501.1:n.757-10del
NM_001354573.2:c.676-10del	NP_001341502.1:n.676-10del