Canonical Allele Identifier: CA2429833919

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432331A= , CM000685.2:g.53432331A=	GRCh38
NC_000023.10:g.53459279A= , CM000685.1:g.53459279A=	GRCh37
NC_000023.9:g.53476004A=	NCBI36
NG_008153.1:g.7045T= , LRG_450:g.7045T=
NG_033076.2:g.14477A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.417T=
ENST00000682365.1:n.1608T=
ENST00000684251.1:n.117T=
ENST00000684503.1:n.438T=
ENST00000684692.1:c.273T=	ENSP00000506792.1:p.Cys91=
ENST00000168216.11:c.273T= MANE Select	ENSP00000168216.6:p.Cys91=
ENST00000168216.10:c.273T=	ENSP00000168216.6:p.Cys91=
ENST00000375298.4:c.273T=	ENSP00000364447.4:p.Cys91=
ENST00000375304.9:c.273T=	ENSP00000364453.5:p.Cys91=
ENST00000495986.1:n.405T=
NM_001037811.2:c.273T= , LRG_450t2:c.273T=	NP_001032900.1:p.Cys91=
NM_004493.2:c.273T= , LRG_450t1:c.273T=	NP_004484.1:p.Cys91=
NM_004493.3:c.273T= MANE Select	NP_004484.1:p.Cys91=