Canonical Allele Identifier: CA2429833912

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432318C= , CM000685.2:g.53432318C=	GRCh38
NC_000023.10:g.53459266C= , CM000685.1:g.53459266C=	GRCh37
NC_000023.9:g.53475991C=	NCBI36
NG_008153.1:g.7058G= , LRG_450:g.7058G=
NG_033076.2:g.14464C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.430G=
ENST00000682365.1:n.1621G=
ENST00000684251.1:n.130G=
ENST00000684503.1:n.451G=
ENST00000684692.1:c.286G=	ENSP00000506792.1:p.Val96=
ENST00000168216.11:c.286G= MANE Select	ENSP00000168216.6:p.Val96=
ENST00000168216.10:c.286G=	ENSP00000168216.6:p.Val96=
ENST00000375298.4:c.286G=	ENSP00000364447.4:p.Val96=
ENST00000375304.9:c.286G=	ENSP00000364453.5:p.Val96=
ENST00000477706.1:n.5G=
ENST00000495986.1:n.418G=
NM_001037811.2:c.286G= , LRG_450t2:c.286G=	NP_001032900.1:p.Val96=
NM_004493.2:c.286G= , LRG_450t1:c.286G=	NP_004484.1:p.Val96=
NM_004493.3:c.286G= MANE Select	NP_004484.1:p.Val96=