Canonical Allele Identifier: CA2429833691

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53431556T= , CM000685.2:g.53431556T=	GRCh38
NC_000023.10:g.53458504T= , CM000685.1:g.53458504T=	GRCh37
NC_000023.9:g.53475229T=	NCBI36
NG_008153.1:g.7820A= , LRG_450:g.7820A=
NG_033076.2:g.13702T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.751A=
ENST00000682365.1:n.2383A=
ENST00000684251.1:n.762A=
ENST00000684503.1:n.799A=
ENST00000684692.1:c.*183A=	ENSP00000506792.1:n.*183A=
ENST00000168216.11:c.634A= MANE Select	ENSP00000168216.6:p.Lys212=
ENST00000168216.10:c.634A=	ENSP00000168216.6:p.Lys212=
ENST00000375298.4:c.*15A=	ENSP00000364447.4:n.*15A=
ENST00000375304.9:c.607A=	ENSP00000364453.5:p.Lys203=
ENST00000477706.1:n.258A=
NM_001037811.2:c.607A= , LRG_450t2:c.607A=	NP_001032900.1:p.Lys203=
NM_004493.2:c.634A= , LRG_450t1:c.634A=	NP_004484.1:p.Lys212=
NM_004493.3:c.634A= MANE Select	NP_004484.1:p.Lys212=