Canonical Allele Identifier: CA2429833942

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432422A= , CM000685.2:g.53432422A=	GRCh38
NC_000023.10:g.53459370A= , CM000685.1:g.53459370A=	GRCh37
NC_000023.9:g.53476095A=	NCBI36
NG_008153.1:g.6954T= , LRG_450:g.6954T=
NG_033076.2:g.14568A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.337-11T=
ENST00000682365.1:n.1517T=
ENST00000684251.1:n.26T=
ENST00000684503.1:n.347T=
ENST00000684692.1:c.193-11T=	ENSP00000506792.1:n.193-11T=
ENST00000168216.11:c.193-11T= MANE Select	ENSP00000168216.6:n.193-11T=
ENST00000168216.10:c.193-11T=	ENSP00000168216.6:n.193-11T=
ENST00000375298.4:c.193-11T=	ENSP00000364447.4:n.193-11T=
ENST00000375304.9:c.193-11T=	ENSP00000364453.5:n.193-11T=
ENST00000495986.1:n.325-11T=
NM_001037811.2:c.193-11T= , LRG_450t2:c.193-11T=	NP_001032900.1:n.193-11T=
NM_004493.2:c.193-11T= , LRG_450t1:c.193-11T=	NP_004484.1:n.193-11T=
NM_004493.3:c.193-11T= MANE Select	NP_004484.1:n.193-11T=