Canonical Allele Identifier: CA2739273526

Gene: HSD17B10

Linked Data

• ClinVar Variation Id: 2851210
• ClinVar RCV Id: RCV003691029

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53431605T>C , CM000685.2:g.53431605T>C	GRCh38
NC_000023.10:g.53458553T>C , CM000685.1:g.53458553T>C	GRCh37
NC_000023.9:g.53475278T>C	NCBI36
NG_008153.1:g.7771A>G , LRG_450:g.7771A>G
NG_033076.2:g.13751T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.713-11A>G
ENST00000682365.1:n.2334A>G
ENST00000684251.1:n.713A>G
ENST00000684503.1:n.761-11A>G
ENST00000684692.1:c.*134A>G	ENSP00000506792.1:n.*134A>G
ENST00000168216.11:c.596-11A>G MANE Select	ENSP00000168216.6:n.596-11A>G
ENST00000168216.10:c.596-11A>G	ENSP00000168216.6:n.596-11A>G
ENST00000375298.4:c.487-11A>G	ENSP00000364447.4:n.487-11A>G
ENST00000375304.9:c.569-11A>G	ENSP00000364453.5:n.569-11A>G
ENST00000477706.1:n.220-11A>G
NM_001037811.2:c.569-11A>G , LRG_450t2:c.569-11A>G	NP_001032900.1:n.569-11A>G
NM_004493.2:c.596-11A>G , LRG_450t1:c.596-11A>G	NP_004484.1:n.596-11A>G
NM_004493.3:c.596-11A>G MANE Select	NP_004484.1:n.596-11A>G