Canonical Allele Identifier: CA2429833909

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432304C= , CM000685.2:g.53432304C=	GRCh38
NC_000023.10:g.53459252C= , CM000685.1:g.53459252C=	GRCh37
NC_000023.9:g.53475977C=	NCBI36
NG_008153.1:g.7072G= , LRG_450:g.7072G=
NG_033076.2:g.14450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.444G=
ENST00000682365.1:n.1635G=
ENST00000684251.1:n.144G=
ENST00000684503.1:n.465G=
ENST00000684692.1:c.300G=	ENSP00000506792.1:p.Thr100=
ENST00000168216.11:c.300G= MANE Select	ENSP00000168216.6:p.Thr100=
ENST00000168216.10:c.300G=	ENSP00000168216.6:p.Thr100=
ENST00000375298.4:c.300G=	ENSP00000364447.4:p.Thr100=
ENST00000375304.9:c.300G=	ENSP00000364453.5:p.Thr100=
ENST00000477706.1:n.19G=
ENST00000495986.1:n.432G=
NM_001037811.2:c.300G= , LRG_450t2:c.300G=	NP_001032900.1:p.Thr100=
NM_004493.2:c.300G= , LRG_450t1:c.300G=	NP_004484.1:p.Thr100=
NM_004493.3:c.300G= MANE Select	NP_004484.1:p.Thr100=