Canonical Allele Identifier: CA1233581732

Gene: TPO

Linked Data

• dbSNP Id: rs1673156321

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1504052_1504058del , CM000664.2:g.1504052_1504058del	GRCh38
NC_000002.11:g.1507824_1507830del , CM000664.1:g.1507824_1507830del	GRCh37
NC_000002.10:g.1486831_1486837del	NCBI36
NG_011581.1:g.95590_95596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2491_2497del MANE Select	ENSP00000329869.4:p.Leu831ThrfsTer7
ENST00000329066.8:c.2491_2497del	ENSP00000329869.4:p.Leu831ThrfsTer7
ENST00000345913.8:c.2491_2497del	ENSP00000318820.7:p.Leu831ThrfsTer7
ENST00000346956.7:c.2386+7287_2386+7293del	ENSP00000263886.6:n.2386+7287_2386+7293del
ENST00000382198.5:c.1972_1978del	ENSP00000371633.1:p.Leu658ThrfsTer7
ENST00000382201.7:c.2320_2326del	ENSP00000371636.3:p.Leu774ThrfsTer7
ENST00000422464.5:c.2173+7287_2173+7293del	ENSP00000405788.1:n.2173+7287_2173+7293del
ENST00000425083.3:n.154_160del
ENST00000446278.5:c.915_921del
ENST00000462973.5:n.424+10013_424+10019del
ENST00000469607.3:c.808+7287_808+7293del	ENSP00000419461.1:n.808+7287_808+7293del
ENST00000497517.6:n.782_788del
NM_000547.5:c.2491_2497del	NP_000538.3:p.Leu831ThrfsTer7
NM_001206744.1:c.2491_2497del	NP_001193673.1:p.Leu831ThrfsTer7
NM_001206745.1:c.2320_2326del	NP_001193674.1:p.Leu774ThrfsTer7
NM_175719.3:c.2320_2326del	NP_783650.1:p.Leu774ThrfsTer7
NM_175721.3:c.2386+7287_2386+7293del	NP_783652.1:n.2386+7287_2386+7293del
NM_175722.3:c.1972_1978del	NP_783653.1:p.Leu658ThrfsTer7
XM_011510379.1:c.2386+7287_2386+7293del	XP_011508681.1:n.2386+7287_2386+7293del
XM_011510380.1:c.2491_2497del	XP_011508682.1:p.Leu831ThrfsTer7
XM_011510381.1:c.2215+7287_2215+7293del	XP_011508683.1:n.2215+7287_2215+7293del
XR_922681.1:n.2492_2498del
XM_011510380.3:c.2527_2533del	XP_011508682.2:p.Leu843ThrfsTer7
XM_024453085.1:c.2422+7287_2422+7293del	XP_024308853.1:n.2422+7287_2422+7293del
XM_024453086.1:c.2527_2533del	XP_024308854.1:p.Leu843ThrfsTer7
XM_024453087.1:c.2386+7287_2386+7293del	XP_024308855.1:n.2386+7287_2386+7293del
XM_024453088.1:c.2386+7287_2386+7293del	XP_024308856.1:n.2386+7287_2386+7293del
XM_024453089.1:c.2386+7287_2386+7293del	XP_024308857.1:n.2386+7287_2386+7293del
XM_024453090.1:c.2422+7287_2422+7293del	XP_024308858.1:n.2422+7287_2422+7293del
XM_024453091.1:c.2356_2362del	XP_024308859.1:p.Leu786ThrfsTer7
XM_024453092.1:c.2251+7287_2251+7293del	XP_024308860.1:n.2251+7287_2251+7293del
XM_024453093.1:c.2008_2014del	XP_024308861.1:p.Leu670ThrfsTer7
NM_001206744.2:c.2491_2497del MANE Select	NP_001193673.1:p.Leu831ThrfsTer7
NM_000547.6:c.2491_2497del	NP_000538.3:p.Leu831ThrfsTer7
NM_001206745.2:c.2320_2326del	NP_001193674.1:p.Leu774ThrfsTer7
NM_175719.4:c.2320_2326del	NP_783650.1:p.Leu774ThrfsTer7