Canonical Allele Identifier: CA2429833883

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432213_53432216delinsTACC , CM000685.2:g.53432213_53432216delinsTACC	GRCh38
NC_000023.10:g.53459161_53459164delinsTACC , CM000685.1:g.53459161_53459164delinsTACC	GRCh37
NC_000023.9:g.53475886_53475889delinsTACC	NCBI36
NG_008153.1:g.7160_7163delinsGGTA , LRG_450:g.7160_7163delinsGGTA
NG_033076.2:g.14359_14362delinsTACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.501+31_501+34delinsGGTA
ENST00000682365.1:n.1723_1726delinsGGTA
ENST00000684251.1:n.201+31_201+34delinsGGTA
ENST00000684503.1:n.522+31_522+34delinsGGTA
ENST00000684692.1:c.357+31_357+34delinsGGTA	ENSP00000506792.1:n.357+31_357+34delinsGGTA
ENST00000168216.11:c.357+31_357+34delinsGGTA MANE Select	ENSP00000168216.6:n.357+31_357+34delinsGGTA
ENST00000168216.10:c.357+31_357+34delinsGGTA	ENSP00000168216.6:n.357+31_357+34delinsGGTA
ENST00000375298.4:c.357+31_357+34delinsGGTA	ENSP00000364447.4:n.357+31_357+34delinsGGTA
ENST00000375304.9:c.357+31_357+34delinsGGTA	ENSP00000364453.5:n.357+31_357+34delinsGGTA
ENST00000477706.1:n.76+31_76+34delinsGGTA
ENST00000495986.1:n.489+31_489+34delinsGGTA
NM_001037811.2:c.357+31_357+34delinsGGTA , LRG_450t2:c.357+31_357+34delinsGGTA	NP_001032900.1:n.357+31_357+34delinsGGTA
NM_004493.2:c.357+31_357+34delinsGGTA , LRG_450t1:c.357+31_357+34delinsGGTA	NP_004484.1:n.357+31_357+34delinsGGTA
NM_004493.3:c.357+31_357+34delinsGGTA MANE Select	NP_004484.1:n.357+31_357+34delinsGGTA