Canonical Allele Identifier: CA2429833842

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432086G= , CM000685.2:g.53432086G=	GRCh38
NC_000023.10:g.53459034G= , CM000685.1:g.53459034G=	GRCh37
NC_000023.9:g.53475759G=	NCBI36
NG_008153.1:g.7290C= , LRG_450:g.7290C=
NG_033076.2:g.14232G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004493.3:c.388C= MANE Select	NP_004484.1:p.Arg130=
ENST00000168216.11:c.388C= MANE Select	ENSP00000168216.6:p.Arg130=
NM_001037811.2:c.388C= , LRG_450t2:c.388C=	NP_001032900.1:p.Arg130=
NM_004493.2:c.388C= , LRG_450t1:c.388C=	NP_004484.1:p.Arg130=
ENST00000168216.10:c.388C=	ENSP00000168216.6:p.Arg130=
ENST00000375298.4:c.388C=	ENSP00000364447.4:p.Arg130=
ENST00000375304.9:c.388C=	ENSP00000364453.5:p.Arg130=
ENST00000477706.1:n.107C=
ENST00000495986.1:n.520C=
ENST00000495986.2:n.532C=
ENST00000682365.1:n.1853C=
ENST00000684251.1:n.232C=
ENST00000684503.1:n.553C=
ENST00000684692.1:c.388C=	ENSP00000506792.1:p.Arg130=