Canonical Allele Identifier: CA2429833923

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432347T= , CM000685.2:g.53432347T=	GRCh38
NC_000023.10:g.53459295T= , CM000685.1:g.53459295T=	GRCh37
NC_000023.9:g.53476020T=	NCBI36
NG_008153.1:g.7029A= , LRG_450:g.7029A=
NG_033076.2:g.14493T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004493.3:c.257A= MANE Select	NP_004484.1:p.Asp86=
ENST00000168216.11:c.257A= MANE Select	ENSP00000168216.6:p.Asp86=
NM_001037811.2:c.257A= , LRG_450t2:c.257A=	NP_001032900.1:p.Asp86=
NM_004493.2:c.257A= , LRG_450t1:c.257A=	NP_004484.1:p.Asp86=
ENST00000168216.10:c.257A=	ENSP00000168216.6:p.Asp86=
ENST00000375298.4:c.257A=	ENSP00000364447.4:p.Asp86=
ENST00000375304.9:c.257A=	ENSP00000364453.5:p.Asp86=
ENST00000495986.1:n.389A=
ENST00000495986.2:n.401A=
ENST00000682365.1:n.1592A=
ENST00000684251.1:n.101A=
ENST00000684503.1:n.422A=
ENST00000684692.1:c.257A=	ENSP00000506792.1:p.Asp86=