Canonical Allele Identifier: CA2668959008

Gene: AHSG

Linked Data

• gnomAD v4: 3-186618632-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618636del , CM000665.2:g.186618636del	GRCh38
NC_000003.11:g.186336425del , CM000665.1:g.186336425del	GRCh37
NC_000003.10:g.187819119del	NCBI36
NG_011436.1:g.10576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.674del MANE Select	ENSP00000393887.2:p.Lys225SerfsTer21
ENST00000273784.5:c.677del	ENSP00000273784.5:p.Lys226SerfsTer21
ENST00000411641.6:c.674del	ENSP00000393887.2:p.Lys225SerfsTer21
NM_001622.2:c.674del	NP_001613.2:p.Lys225SerfsTer21
NM_001354571.1:c.677del	NP_001341500.1:p.Lys226SerfsTer21
NM_001354572.1:c.671del	NP_001341501.1:p.Lys224SerfsTer21
NM_001354573.1:c.674del	NP_001341502.1:p.Lys225SerfsTer3
NM_001622.3:c.674del	NP_001613.2:p.Lys225SerfsTer21
NM_001622.4:c.674del MANE Select	NP_001613.2:p.Lys225SerfsTer21
NM_001354571.2:c.677del	NP_001341500.1:p.Lys226SerfsTer21
NM_001354572.2:c.671del	NP_001341501.1:p.Lys224SerfsTer21
NM_001354573.2:c.674del	NP_001341502.1:p.Lys225SerfsTer3