Canonical Allele Identifier: CA413152734

Gene: HSD17B10

Linked Data

• MyVariant Identifiers: chrX:g.53459220A>T (hg19) ; chrX:g.53432272A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432272A>T , CM000685.2:g.53432272A>T	GRCh38
NC_000023.10:g.53459220A>T , CM000685.1:g.53459220A>T	GRCh37
NC_000023.9:g.53475945A>T	NCBI36
NG_008153.1:g.7104T>A , LRG_450:g.7104T>A
NG_033076.2:g.14418A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.476T>A
ENST00000682365.1:n.1667T>A
ENST00000684251.1:n.176T>A
ENST00000684503.1:n.497T>A
ENST00000684692.1:c.332T>A	ENSP00000506792.1:p.Leu111Ter
ENST00000168216.11:c.332T>A MANE Select	ENSP00000168216.6:p.Leu111Ter
ENST00000168216.10:c.332T>A	ENSP00000168216.6:p.Leu111Ter
ENST00000375298.4:c.332T>A	ENSP00000364447.4:p.Leu111Ter
ENST00000375304.9:c.332T>A	ENSP00000364453.5:p.Leu111Ter
ENST00000477706.1:n.51T>A
ENST00000495986.1:n.464T>A
NM_001037811.2:c.332T>A , LRG_450t2:c.332T>A	NP_001032900.1:p.Leu111Ter
NM_004493.2:c.332T>A , LRG_450t1:c.332T>A	NP_004484.1:p.Leu111Ter
NM_004493.3:c.332T>A MANE Select	NP_004484.1:p.Leu111Ter