Canonical Allele Identifier: CA2668958986

Gene: AHSG

Linked Data

• gnomAD v4: 3-186618558-TGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618560_186618562del , CM000665.2:g.186618560_186618562del	GRCh38
NC_000003.11:g.186336349_186336351del , CM000665.1:g.186336349_186336351del	GRCh37
NC_000003.10:g.187819043_187819045del	NCBI36
NG_011436.1:g.10500_10502del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.598_600del MANE Select	ENSP00000393887.2:p.Glu200del
ENST00000273784.5:c.601_603del	ENSP00000273784.5:p.Glu201del
ENST00000411641.6:c.598_600del	ENSP00000393887.2:p.Glu200del
NM_001622.2:c.598_600del	NP_001613.2:p.Glu200del
NM_001354571.1:c.601_603del	NP_001341500.1:p.Glu201del
NM_001354572.1:c.595_597del	NP_001341501.1:p.Glu199del
NM_001354573.1:c.598_600del	NP_001341502.1:p.Glu200del
NM_001622.3:c.598_600del	NP_001613.2:p.Glu200del
NM_001622.4:c.598_600del MANE Select	NP_001613.2:p.Glu200del
NM_001354571.2:c.601_603del	NP_001341500.1:p.Glu201del
NM_001354572.2:c.595_597del	NP_001341501.1:p.Glu199del
NM_001354573.2:c.598_600del	NP_001341502.1:p.Glu200del