Canonical Allele Identifier: CA413153417

Gene: HSD17B10

Linked Data

• MyVariant Identifiers: chrX:g.53459341C>A (hg19) ; chrX:g.53432393C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432393C>A , CM000685.2:g.53432393C>A	GRCh38
NC_000023.10:g.53459341C>A , CM000685.1:g.53459341C>A	GRCh37
NC_000023.9:g.53476066C>A	NCBI36
NG_008153.1:g.6983G>T , LRG_450:g.6983G>T
NG_033076.2:g.14539C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.355G>T
ENST00000682365.1:n.1546G>T
ENST00000684251.1:n.55G>T
ENST00000684503.1:n.376G>T
ENST00000684692.1:c.211G>T	ENSP00000506792.1:p.Val71Leu
ENST00000168216.11:c.211G>T MANE Select	ENSP00000168216.6:p.Val71Leu
ENST00000168216.10:c.211G>T	ENSP00000168216.6:p.Val71Leu
ENST00000375298.4:c.211G>T	ENSP00000364447.4:p.Val71Leu
ENST00000375304.9:c.211G>T	ENSP00000364453.5:p.Val71Leu
ENST00000495986.1:n.343G>T
NM_001037811.2:c.211G>T , LRG_450t2:c.211G>T	NP_001032900.1:p.Val71Leu
NM_004493.2:c.211G>T , LRG_450t1:c.211G>T	NP_004484.1:p.Val71Leu
NM_004493.3:c.211G>T MANE Select	NP_004484.1:p.Val71Leu