Canonical Allele Identifier: CA2429833668

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53431450T= , CM000685.2:g.53431450T=	GRCh38
NC_000023.10:g.53458398T= , CM000685.1:g.53458398T=	GRCh37
NC_000023.9:g.53475123T=	NCBI36
NG_008153.1:g.7926A= , LRG_450:g.7926A=
NG_033076.2:g.13596T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.857A=
ENST00000682365.1:n.2489A=
ENST00000684251.1:n.868A=
ENST00000684692.1:c.*289A=	ENSP00000506792.1:n.*289A=
ENST00000168216.11:c.740A= MANE Select	ENSP00000168216.6:p.Asn247=
ENST00000168216.10:c.740A=	ENSP00000168216.6:p.Asn247=
ENST00000375298.4:c.*121A=	ENSP00000364447.4:n.*121A=
ENST00000375304.9:c.713A=	ENSP00000364453.5:p.Asn238=
ENST00000477706.1:n.364A=
NM_001037811.2:c.713A= , LRG_450t2:c.713A=	NP_001032900.1:p.Asn238=
NM_004493.2:c.740A= , LRG_450t1:c.740A=	NP_004484.1:p.Asn247=
NM_004493.3:c.740A= MANE Select	NP_004484.1:p.Asn247=