Canonical Allele Identifier: CA1427018754

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618671_186618672delinsCG , CM000665.2:g.186618671_186618672delinsCG	GRCh38
NC_000003.11:g.186336460_186336461delinsCG , CM000665.1:g.186336460_186336461delinsCG	GRCh37
NC_000003.10:g.187819154_187819155delinsCG	NCBI36
NG_011436.1:g.10611_10612delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.675+34_675+35delinsCG MANE Select	ENSP00000393887.2:n.675+34_675+35delinsCG
ENST00000273784.5:c.678+34_678+35delinsCG	ENSP00000273784.5:n.678+34_678+35delinsCG
ENST00000411641.6:c.675+34_675+35delinsCG	ENSP00000393887.2:n.675+34_675+35delinsCG
NM_001622.2:c.675+34_675+35delinsCG	NP_001613.2:n.675+34_675+35delinsCG
NM_001354571.1:c.678+34_678+35delinsCG	NP_001341500.1:n.678+34_678+35delinsCG
NM_001354572.1:c.672+34_672+35delinsCG	NP_001341501.1:n.672+34_672+35delinsCG
NM_001354573.1:c.675+34_675+35delinsCG	NP_001341502.1:n.675+34_675+35delinsCG
NM_001622.3:c.675+34_675+35delinsCG	NP_001613.2:n.675+34_675+35delinsCG
NM_001622.4:c.675+34_675+35delinsCG MANE Select	NP_001613.2:n.675+34_675+35delinsCG
NM_001354571.2:c.678+34_678+35delinsCG	NP_001341500.1:n.678+34_678+35delinsCG
NM_001354572.2:c.672+34_672+35delinsCG	NP_001341501.1:n.672+34_672+35delinsCG
NM_001354573.2:c.675+34_675+35delinsCG	NP_001341502.1:n.675+34_675+35delinsCG