Canonical Allele Identifier: CA413153101

Gene: HSD17B10

Linked Data

• MyVariant Identifiers: chrX:g.53459286A>C (hg19) ; chrX:g.53432338A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432338A>C , CM000685.2:g.53432338A>C	GRCh38
NC_000023.10:g.53459286A>C , CM000685.1:g.53459286A>C	GRCh37
NC_000023.9:g.53476011A>C	NCBI36
NG_008153.1:g.7038T>G , LRG_450:g.7038T>G
NG_033076.2:g.14484A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.410T>G
ENST00000682365.1:n.1601T>G
ENST00000684251.1:n.110T>G
ENST00000684503.1:n.431T>G
ENST00000684692.1:c.266T>G	ENSP00000506792.1:p.Val89Gly
ENST00000168216.11:c.266T>G MANE Select	ENSP00000168216.6:p.Val89Gly
ENST00000168216.10:c.266T>G	ENSP00000168216.6:p.Val89Gly
ENST00000375298.4:c.266T>G	ENSP00000364447.4:p.Val89Gly
ENST00000375304.9:c.266T>G	ENSP00000364453.5:p.Val89Gly
ENST00000495986.1:n.398T>G
NM_001037811.2:c.266T>G , LRG_450t2:c.266T>G	NP_001032900.1:p.Val89Gly
NM_004493.2:c.266T>G , LRG_450t1:c.266T>G	NP_004484.1:p.Val89Gly
NM_004493.3:c.266T>G MANE Select	NP_004484.1:p.Val89Gly