Canonical Allele Identifier: CA1427018725

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618603_186618604delinsCA , CM000665.2:g.186618603_186618604delinsCA	GRCh38
NC_000003.11:g.186336392_186336393delinsCA , CM000665.1:g.186336392_186336393delinsCA	GRCh37
NC_000003.10:g.187819086_187819087delinsCA	NCBI36
NG_011436.1:g.10543_10544delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.641_642delinsCA MANE Select	ENSP00000393887.2:p.Thr214=
ENST00000273784.5:c.644_645delinsCA	ENSP00000273784.5:p.Thr215=
ENST00000411641.6:c.641_642delinsCA	ENSP00000393887.2:p.Thr214=
NM_001622.2:c.641_642delinsCA	NP_001613.2:p.Thr214=
NM_001354571.1:c.644_645delinsCA	NP_001341500.1:p.Thr215=
NM_001354572.1:c.638_639delinsCA	NP_001341501.1:p.Thr213=
NM_001354573.1:c.641_642delinsCA	NP_001341502.1:p.Thr214=
NM_001622.3:c.641_642delinsCA	NP_001613.2:p.Thr214=
NM_001622.4:c.641_642delinsCA MANE Select	NP_001613.2:p.Thr214=
NM_001354571.2:c.644_645delinsCA	NP_001341500.1:p.Thr215=
NM_001354572.2:c.638_639delinsCA	NP_001341501.1:p.Thr213=
NM_001354573.2:c.641_642delinsCA	NP_001341502.1:p.Thr214=