Canonical Allele Identifier: CA2579616361

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432238_53432239del , CM000685.2:g.53432238_53432239del	GRCh38
NC_000023.10:g.53459186_53459187del , CM000685.1:g.53459186_53459187del	GRCh37
NC_000023.9:g.53475911_53475912del	NCBI36
NG_008153.1:g.7137_7138del , LRG_450:g.7137_7138del
NG_033076.2:g.14384_14385del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.501+8_501+9del
ENST00000682365.1:n.1700_1701del
ENST00000684251.1:n.201+8_201+9del
ENST00000684503.1:n.522+8_522+9del
ENST00000684692.1:c.357+8_357+9del	ENSP00000506792.1:n.357+8_357+9del
ENST00000168216.11:c.357+8_357+9del MANE Select	ENSP00000168216.6:n.357+8_357+9del
ENST00000168216.10:c.357+8_357+9del	ENSP00000168216.6:n.357+8_357+9del
ENST00000375298.4:c.357+8_357+9del	ENSP00000364447.4:n.357+8_357+9del
ENST00000375304.9:c.357+8_357+9del	ENSP00000364453.5:n.357+8_357+9del
ENST00000477706.1:n.76+8_76+9del
ENST00000495986.1:n.489+8_489+9del
NM_001037811.2:c.357+8_357+9del , LRG_450t2:c.357+8_357+9del	NP_001032900.1:n.357+8_357+9del
NM_004493.2:c.357+8_357+9del , LRG_450t1:c.357+8_357+9del	NP_004484.1:n.357+8_357+9del
NM_004493.3:c.357+8_357+9del MANE Select	NP_004484.1:n.357+8_357+9del