Canonical Allele Identifier: CA2693808000

Gene: HSD17B10

Linked Data

• gnomAD v4: X-53432179-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432179A>C , CM000685.2:g.53432179A>C	GRCh38
NC_000023.10:g.53459127A>C , CM000685.1:g.53459127A>C	GRCh37
NC_000023.9:g.53475852A>C	NCBI36
NG_008153.1:g.7197T>G , LRG_450:g.7197T>G
NG_033076.2:g.14325A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.502-63T>G
ENST00000682365.1:n.1760T>G
ENST00000684251.1:n.202-63T>G
ENST00000684503.1:n.523-63T>G
ENST00000684692.1:c.358-63T>G	ENSP00000506792.1:n.358-63T>G
ENST00000168216.11:c.358-63T>G MANE Select	ENSP00000168216.6:n.358-63T>G
ENST00000168216.10:c.358-63T>G	ENSP00000168216.6:n.358-63T>G
ENST00000375298.4:c.358-63T>G	ENSP00000364447.4:n.358-63T>G
ENST00000375304.9:c.358-63T>G	ENSP00000364453.5:n.358-63T>G
ENST00000477706.1:n.77-63T>G
ENST00000495986.1:n.490-63T>G
NM_001037811.2:c.358-63T>G , LRG_450t2:c.358-63T>G	NP_001032900.1:n.358-63T>G
NM_004493.2:c.358-63T>G , LRG_450t1:c.358-63T>G	NP_004484.1:n.358-63T>G
NM_004493.3:c.358-63T>G MANE Select	NP_004484.1:n.358-63T>G