Canonical Allele Identifier: CA413152603

Gene: HSD17B10

Linked Data

• MyVariant Identifiers: chrX:g.53459197C>A (hg19) ; chrX:g.53432249C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432249C>A , CM000685.2:g.53432249C>A	GRCh38
NC_000023.10:g.53459197C>A , CM000685.1:g.53459197C>A	GRCh37
NC_000023.9:g.53475922C>A	NCBI36
NG_008153.1:g.7127G>T , LRG_450:g.7127G>T
NG_033076.2:g.14395C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.499G>T
ENST00000682365.1:n.1690G>T
ENST00000684251.1:n.199G>T
ENST00000684503.1:n.520G>T
ENST00000684692.1:c.355G>T	ENSP00000506792.1:p.Asp119Tyr
ENST00000168216.11:c.355G>T MANE Select	ENSP00000168216.6:p.Asp119Tyr
ENST00000168216.10:c.355G>T	ENSP00000168216.6:p.Asp119Tyr
ENST00000375298.4:c.355G>T	ENSP00000364447.4:p.Asp119Tyr
ENST00000375304.9:c.355G>T	ENSP00000364453.5:p.Asp119Tyr
ENST00000477706.1:n.74G>T
ENST00000495986.1:n.487G>T
NM_001037811.2:c.355G>T , LRG_450t2:c.355G>T	NP_001032900.1:p.Asp119Tyr
NM_004493.2:c.355G>T , LRG_450t1:c.355G>T	NP_004484.1:p.Asp119Tyr
NM_004493.3:c.355G>T MANE Select	NP_004484.1:p.Asp119Tyr