Canonical Allele Identifier: CA2693808004

Gene: HSD17B10

Linked Data

• gnomAD v4: X-53432194-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432194A>G , CM000685.2:g.53432194A>G	GRCh38
NC_000023.10:g.53459142A>G , CM000685.1:g.53459142A>G	GRCh37
NC_000023.9:g.53475867A>G	NCBI36
NG_008153.1:g.7182T>C , LRG_450:g.7182T>C
NG_033076.2:g.14340A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.501+53T>C
ENST00000682365.1:n.1745T>C
ENST00000684251.1:n.201+53T>C
ENST00000684503.1:n.522+53T>C
ENST00000684692.1:c.357+53T>C	ENSP00000506792.1:n.357+53T>C
ENST00000168216.11:c.357+53T>C MANE Select	ENSP00000168216.6:n.357+53T>C
ENST00000168216.10:c.357+53T>C	ENSP00000168216.6:n.357+53T>C
ENST00000375298.4:c.357+53T>C	ENSP00000364447.4:n.357+53T>C
ENST00000375304.9:c.357+53T>C	ENSP00000364453.5:n.357+53T>C
ENST00000477706.1:n.76+53T>C
ENST00000495986.1:n.489+53T>C
NM_001037811.2:c.357+53T>C , LRG_450t2:c.357+53T>C	NP_001032900.1:n.357+53T>C
NM_004493.2:c.357+53T>C , LRG_450t1:c.357+53T>C	NP_004484.1:n.357+53T>C
NM_004493.3:c.357+53T>C MANE Select	NP_004484.1:n.357+53T>C