Canonical Allele Identifier: CA516429134

Gene: HSD17B10

Linked Data

• MyVariant Identifiers: chrX:g.53459276T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432328T>A , CM000685.2:g.53432328T>A	GRCh38
NC_000023.10:g.53459276T>A , CM000685.1:g.53459276T>A	GRCh37
NC_000023.9:g.53476001T>A	NCBI36
NG_008153.1:g.7048A>T , LRG_450:g.7048A>T
NG_033076.2:g.14474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.420A>T
ENST00000682365.1:n.1611A>T
ENST00000684251.1:n.120A>T
ENST00000684503.1:n.441A>T
ENST00000684692.1:c.276A>T	ENSP00000506792.1:p.Ala92=
ENST00000168216.11:c.276A>T MANE Select	ENSP00000168216.6:p.Ala92=
ENST00000168216.10:c.276A>T	ENSP00000168216.6:p.Ala92=
ENST00000375298.4:c.276A>T	ENSP00000364447.4:p.Ala92=
ENST00000375304.9:c.276A>T	ENSP00000364453.5:p.Ala92=
ENST00000495986.1:n.408A>T
NM_001037811.2:c.276A>T , LRG_450t2:c.276A>T	NP_001032900.1:p.Ala92=
NM_004493.2:c.276A>T , LRG_450t1:c.276A>T	NP_004484.1:p.Ala92=
NM_004493.3:c.276A>T MANE Select	NP_004484.1:p.Ala92=