Canonical Allele Identifier: CA2429833892

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432244T= , CM000685.2:g.53432244T=	GRCh38
NC_000023.10:g.53459192T= , CM000685.1:g.53459192T=	GRCh37
NC_000023.9:g.53475917T=	NCBI36
NG_008153.1:g.7132A= , LRG_450:g.7132A=
NG_033076.2:g.14390T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.501+3A=
ENST00000682365.1:n.1695A=
ENST00000684251.1:n.201+3A=
ENST00000684503.1:n.522+3A=
ENST00000684692.1:c.357+3A=	ENSP00000506792.1:n.357+3A=
ENST00000168216.11:c.357+3A= MANE Select	ENSP00000168216.6:n.357+3A=
ENST00000168216.10:c.357+3A=	ENSP00000168216.6:n.357+3A=
ENST00000375298.4:c.357+3A=	ENSP00000364447.4:n.357+3A=
ENST00000375304.9:c.357+3A=	ENSP00000364453.5:n.357+3A=
ENST00000477706.1:n.76+3A=
ENST00000495986.1:n.489+3A=
NM_001037811.2:c.357+3A= , LRG_450t2:c.357+3A=	NP_001032900.1:n.357+3A=
NM_004493.2:c.357+3A= , LRG_450t1:c.357+3A=	NP_004484.1:n.357+3A=
NM_004493.3:c.357+3A= MANE Select	NP_004484.1:n.357+3A=