Canonical Allele Identifier: CA2579616358

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432219T>C , CM000685.2:g.53432219T>C	GRCh38
NC_000023.10:g.53459167T>C , CM000685.1:g.53459167T>C	GRCh37
NC_000023.9:g.53475892T>C	NCBI36
NG_008153.1:g.7157A>G , LRG_450:g.7157A>G
NG_033076.2:g.14365T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.501+28A>G
ENST00000682365.1:n.1720A>G
ENST00000684251.1:n.201+28A>G
ENST00000684503.1:n.522+28A>G
ENST00000684692.1:c.357+28A>G	ENSP00000506792.1:n.357+28A>G
ENST00000168216.11:c.357+28A>G MANE Select	ENSP00000168216.6:n.357+28A>G
ENST00000168216.10:c.357+28A>G	ENSP00000168216.6:n.357+28A>G
ENST00000375298.4:c.357+28A>G	ENSP00000364447.4:n.357+28A>G
ENST00000375304.9:c.357+28A>G	ENSP00000364453.5:n.357+28A>G
ENST00000477706.1:n.76+28A>G
ENST00000495986.1:n.489+28A>G
NM_001037811.2:c.357+28A>G , LRG_450t2:c.357+28A>G	NP_001032900.1:n.357+28A>G
NM_004493.2:c.357+28A>G , LRG_450t1:c.357+28A>G	NP_004484.1:n.357+28A>G
NM_004493.3:c.357+28A>G MANE Select	NP_004484.1:n.357+28A>G