Canonical Allele Identifier: CA2668956814

Gene: AHSG

Linked Data

• gnomAD v4: 3-186620635-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620636del , CM000665.2:g.186620636del	GRCh38
NC_000003.11:g.186338425del , CM000665.1:g.186338425del	GRCh37
NC_000003.10:g.187821119del	NCBI36
NG_011436.1:g.12576del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.810del MANE Select	ENSP00000393887.2:p.Val272TrpfsTer?
ENST00000273784.5:c.813del	ENSP00000273784.5:p.Val273TrpfsTer?
ENST00000411641.6:c.810del	ENSP00000393887.2:p.Val272TrpfsTer?
NM_001622.2:c.810del	NP_001613.2:p.Val272TrpfsTer?
NM_001354571.1:c.813del	NP_001341500.1:p.Val273TrpfsTer?
NM_001354572.1:c.807del	NP_001341501.1:p.Val271TrpfsTer?
NM_001354573.1:c.726del	NP_001341502.1:p.Val244TrpfsTer?
NM_001622.3:c.810del	NP_001613.2:p.Val272TrpfsTer?
NM_001622.4:c.810del MANE Select	NP_001613.2:p.Val272TrpfsTer?
NM_001354571.2:c.813del	NP_001341500.1:p.Val273TrpfsTer?
NM_001354572.2:c.807del	NP_001341501.1:p.Val271TrpfsTer?
NM_001354573.2:c.726del	NP_001341502.1:p.Val244TrpfsTer?