Canonical Allele Identifier: CA2499856203

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432436T>G , CM000685.2:g.53432436T>G	GRCh38
NC_000023.10:g.53459384T>G , CM000685.1:g.53459384T>G	GRCh37
NC_000023.9:g.53476109T>G	NCBI36
NG_008153.1:g.6940A>C , LRG_450:g.6940A>C
NG_033076.2:g.14582T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.337-25A>C
ENST00000682365.1:n.1503A>C
ENST00000684251.1:n.12A>C
ENST00000684503.1:n.333A>C
ENST00000684692.1:c.193-25A>C	ENSP00000506792.1:n.193-25A>C
ENST00000168216.11:c.193-25A>C MANE Select	ENSP00000168216.6:n.193-25A>C
ENST00000168216.10:c.193-25A>C	ENSP00000168216.6:n.193-25A>C
ENST00000375298.4:c.193-25A>C	ENSP00000364447.4:n.193-25A>C
ENST00000375304.9:c.193-25A>C	ENSP00000364453.5:n.193-25A>C
ENST00000495986.1:n.325-25A>C
NM_001037811.2:c.193-25A>C , LRG_450t2:c.193-25A>C	NP_001032900.1:n.193-25A>C
NM_004493.2:c.193-25A>C , LRG_450t1:c.193-25A>C	NP_004484.1:n.193-25A>C
NM_004493.3:c.193-25A>C MANE Select	NP_004484.1:n.193-25A>C