Canonical Allele Identifier: CA2429833911

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432312T= , CM000685.2:g.53432312T=	GRCh38
NC_000023.10:g.53459260T= , CM000685.1:g.53459260T=	GRCh37
NC_000023.9:g.53475985T=	NCBI36
NG_008153.1:g.7064A= , LRG_450:g.7064A=
NG_033076.2:g.14458T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.436A=
ENST00000682365.1:n.1627A=
ENST00000684251.1:n.136A=
ENST00000684503.1:n.457A=
ENST00000684692.1:c.292A=	ENSP00000506792.1:p.Ser98=
ENST00000168216.11:c.292A= MANE Select	ENSP00000168216.6:p.Ser98=
ENST00000168216.10:c.292A=	ENSP00000168216.6:p.Ser98=
ENST00000375298.4:c.292A=	ENSP00000364447.4:p.Ser98=
ENST00000375304.9:c.292A=	ENSP00000364453.5:p.Ser98=
ENST00000477706.1:n.11A=
ENST00000495986.1:n.424A=
NM_001037811.2:c.292A= , LRG_450t2:c.292A=	NP_001032900.1:p.Ser98=
NM_004493.2:c.292A= , LRG_450t1:c.292A=	NP_004484.1:p.Ser98=
NM_004493.3:c.292A= MANE Select	NP_004484.1:p.Ser98=