Canonical Allele Identifier: CA2237486467

Gene: HSD17B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82095585_82095586delinsCA , CM000678.2:g.82095585_82095586delinsCA	GRCh38
NC_000016.9:g.82129190_82129191delinsCA , CM000678.1:g.82129190_82129191delinsCA	GRCh37
NC_000016.8:g.80686691_80686692delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000199936.9:c.803-2490_803-2489delinsCA MANE Select	ENSP00000199936.4:n.803-2490_803-2489delinsCA
ENST00000199936.8:c.803-2490_803-2489delinsCA	ENSP00000199936.4:n.803-2490_803-2489delinsCA
ENST00000566838.2:c.4976_4977delinsCA	ENSP00000456471.1:n.4976_4977delinsCA
ENST00000568090.5:c.395-2490_395-2489delinsCA	ENSP00000456529.1:n.395-2490_395-2489delinsCA
NM_002153.2:c.803-2490_803-2489delinsCA	NP_002144.1:n.803-2490_803-2489delinsCA
XR_001751898.2:n.1021-2490_1021-2489delinsCA
NM_002153.3:c.803-2490_803-2489delinsCA MANE Select	NP_002144.1:n.803-2490_803-2489delinsCA