Canonical Allele Identifier: CA516429313

Gene: HSD17B10

Linked Data

• MyVariant Identifiers: chrX:g.53459354G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432406G>C , CM000685.2:g.53432406G>C	GRCh38
NC_000023.10:g.53459354G>C , CM000685.1:g.53459354G>C	GRCh37
NC_000023.9:g.53476079G>C	NCBI36
NG_008153.1:g.6970C>G , LRG_450:g.6970C>G
NG_033076.2:g.14552G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.342C>G
ENST00000682365.1:n.1533C>G
ENST00000684251.1:n.42C>G
ENST00000684503.1:n.363C>G
ENST00000684692.1:c.198C>G	ENSP00000506792.1:p.Thr66=
ENST00000168216.11:c.198C>G MANE Select	ENSP00000168216.6:p.Thr66=
ENST00000168216.10:c.198C>G	ENSP00000168216.6:p.Thr66=
ENST00000375298.4:c.198C>G	ENSP00000364447.4:p.Thr66=
ENST00000375304.9:c.198C>G	ENSP00000364453.5:p.Thr66=
ENST00000495986.1:n.330C>G
NM_001037811.2:c.198C>G , LRG_450t2:c.198C>G	NP_001032900.1:p.Thr66=
NM_004493.2:c.198C>G , LRG_450t1:c.198C>G	NP_004484.1:p.Thr66=
NM_004493.3:c.198C>G MANE Select	NP_004484.1:p.Thr66=