Canonical Allele Identifier: CA2429833665

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53431445C= , CM000685.2:g.53431445C=	GRCh38
NC_000023.10:g.53458393C= , CM000685.1:g.53458393C=	GRCh37
NC_000023.9:g.53475118C=	NCBI36
NG_008153.1:g.7931G= , LRG_450:g.7931G=
NG_033076.2:g.13591C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004493.3:c.745G= MANE Select	NP_004484.1:p.Glu249=
ENST00000168216.11:c.745G= MANE Select	ENSP00000168216.6:p.Glu249=
NM_001037811.2:c.718G= , LRG_450t2:c.718G=	NP_001032900.1:p.Glu240=
NM_004493.2:c.745G= , LRG_450t1:c.745G=	NP_004484.1:p.Glu249=
ENST00000168216.10:c.745G=	ENSP00000168216.6:p.Glu249=
ENST00000375298.4:c.*126G=	ENSP00000364447.4:n.*126G=
ENST00000375304.9:c.718G=	ENSP00000364453.5:p.Glu240=
ENST00000477706.1:n.369G=
ENST00000495986.2:n.862G=
ENST00000682365.1:n.2494G=
ENST00000684251.1:n.873G=
ENST00000684692.1:c.*294G=	ENSP00000506792.1:n.*294G=