Canonical Allele Identifier: CA2429833847

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432110G= , CM000685.2:g.53432110G=	GRCh38
NC_000023.10:g.53459058G= , CM000685.1:g.53459058G=	GRCh37
NC_000023.9:g.53475783G=	NCBI36
NG_008153.1:g.7266C= , LRG_450:g.7266C=
NG_033076.2:g.14256G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.508C=
ENST00000682365.1:n.1829C=
ENST00000684251.1:n.208C=
ENST00000684503.1:n.529C=
ENST00000684692.1:c.364C=	ENSP00000506792.1:p.Leu122=
ENST00000168216.11:c.364C= MANE Select	ENSP00000168216.6:p.Leu122=
ENST00000168216.10:c.364C=	ENSP00000168216.6:p.Leu122=
ENST00000375298.4:c.364C=	ENSP00000364447.4:p.Leu122=
ENST00000375304.9:c.364C=	ENSP00000364453.5:p.Leu122=
ENST00000477706.1:n.83C=
ENST00000495986.1:n.496C=
NM_001037811.2:c.364C= , LRG_450t2:c.364C=	NP_001032900.1:p.Leu122=
NM_004493.2:c.364C= , LRG_450t1:c.364C=	NP_004484.1:p.Leu122=
NM_004493.3:c.364C= MANE Select	NP_004484.1:p.Leu122=