Canonical Allele Identifier: CA2429833773

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53431819G= , CM000685.2:g.53431819G=	GRCh38
NC_000023.10:g.53458767G= , CM000685.1:g.53458767G=	GRCh37
NC_000023.9:g.53475492G=	NCBI36
NG_008153.1:g.7557C= , LRG_450:g.7557C=
NG_033076.2:g.13965G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004493.3:c.574C= MANE Select	NP_004484.1:p.Arg192=
ENST00000168216.11:c.574C= MANE Select	ENSP00000168216.6:p.Arg192=
NM_001037811.2:c.568+6C= , LRG_450t2:c.568+6C=	NP_001032900.1:n.568+6C=
NM_004493.2:c.574C= , LRG_450t1:c.574C=	NP_004484.1:p.Arg192=
ENST00000168216.10:c.574C=	ENSP00000168216.6:p.Arg192=
ENST00000375298.4:c.486+169C=	ENSP00000364447.4:n.486+169C=
ENST00000375304.9:c.568+6C=	ENSP00000364453.5:n.568+6C=
ENST00000477706.1:n.219+155C=
ENST00000495986.2:n.712+6C=
ENST00000682365.1:n.2120C=
ENST00000684251.1:n.499C=
ENST00000684503.1:n.739C=
ENST00000684692.1:c.574C=	ENSP00000506792.1:p.Arg192=