Canonical Allele Identifier: CA413152919

Gene: HSD17B10

Linked Data

• MyVariant Identifiers: chrX:g.53459254T>C (hg19) ; chrX:g.53432306T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432306T>C , CM000685.2:g.53432306T>C	GRCh38
NC_000023.10:g.53459254T>C , CM000685.1:g.53459254T>C	GRCh37
NC_000023.9:g.53475979T>C	NCBI36
NG_008153.1:g.7070A>G , LRG_450:g.7070A>G
NG_033076.2:g.14452T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.442A>G
ENST00000682365.1:n.1633A>G
ENST00000684251.1:n.142A>G
ENST00000684503.1:n.463A>G
ENST00000684692.1:c.298A>G	ENSP00000506792.1:p.Thr100Ala
ENST00000168216.11:c.298A>G MANE Select	ENSP00000168216.6:p.Thr100Ala
ENST00000168216.10:c.298A>G	ENSP00000168216.6:p.Thr100Ala
ENST00000375298.4:c.298A>G	ENSP00000364447.4:p.Thr100Ala
ENST00000375304.9:c.298A>G	ENSP00000364453.5:p.Thr100Ala
ENST00000477706.1:n.17A>G
ENST00000495986.1:n.430A>G
NM_001037811.2:c.298A>G , LRG_450t2:c.298A>G	NP_001032900.1:p.Thr100Ala
NM_004493.2:c.298A>G , LRG_450t1:c.298A>G	NP_004484.1:p.Thr100Ala
NM_004493.3:c.298A>G MANE Select	NP_004484.1:p.Thr100Ala