Canonical Allele Identifier: CA2237486842

Gene: HSD17B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82095851_82095852delinsCT , CM000678.2:g.82095851_82095852delinsCT	GRCh38
NC_000016.9:g.82129456_82129457delinsCT , CM000678.1:g.82129456_82129457delinsCT	GRCh37
NC_000016.8:g.80686957_80686958delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199936.9:c.803-2224_803-2223delinsCT MANE Select	ENSP00000199936.4:n.803-2224_803-2223delinsCT
ENST00000199936.8:c.803-2224_803-2223delinsCT	ENSP00000199936.4:n.803-2224_803-2223delinsCT
ENST00000566838.2:c.5242_5243delinsCT	ENSP00000456471.1:n.5242_5243delinsCT
ENST00000568090.5:c.395-2224_395-2223delinsCT	ENSP00000456529.1:n.395-2224_395-2223delinsCT
NM_002153.2:c.803-2224_803-2223delinsCT	NP_002144.1:n.803-2224_803-2223delinsCT
XR_001751898.2:n.1021-2224_1021-2223delinsCT
NM_002153.3:c.803-2224_803-2223delinsCT MANE Select	NP_002144.1:n.803-2224_803-2223delinsCT