Canonical Allele Identifier: CA1233581687

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1503971_1503972delinsGC , CM000664.2:g.1503971_1503972delinsGC	GRCh38
NC_000002.11:g.1507743_1507744delinsGC , CM000664.1:g.1507743_1507744delinsGC	GRCh37
NC_000002.10:g.1486750_1486751delinsGC	NCBI36
NG_011581.1:g.95509_95510delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2410_2411delinsGC MANE Select	ENSP00000329869.4:p.Ala804=
ENST00000329066.8:c.2410_2411delinsGC	ENSP00000329869.4:p.Ala804=
ENST00000345913.8:c.2410_2411delinsGC	ENSP00000318820.7:p.Ala804=
ENST00000346956.7:c.2386+7206_2386+7207delinsGC	ENSP00000263886.6:n.2386+7206_2386+7207delinsGC
ENST00000382198.5:c.1891_1892delinsGC	ENSP00000371633.1:p.Ala631=
ENST00000382201.7:c.2239_2240delinsGC	ENSP00000371636.3:p.Ala747=
ENST00000422464.5:c.2173+7206_2173+7207delinsGC	ENSP00000405788.1:n.2173+7206_2173+7207delinsGC
ENST00000425083.3:n.73_74delinsGC
ENST00000446278.5:c.834_835delinsGC
ENST00000462973.5:n.424+9932_424+9933delinsGC
ENST00000469607.3:c.808+7206_808+7207delinsGC	ENSP00000419461.1:n.808+7206_808+7207delinsGC
ENST00000497517.6:n.701_702delinsGC
NM_000547.5:c.2410_2411delinsGC	NP_000538.3:p.Ala804=
NM_001206744.1:c.2410_2411delinsGC	NP_001193673.1:p.Ala804=
NM_001206745.1:c.2239_2240delinsGC	NP_001193674.1:p.Ala747=
NM_175719.3:c.2239_2240delinsGC	NP_783650.1:p.Ala747=
NM_175721.3:c.2386+7206_2386+7207delinsGC	NP_783652.1:n.2386+7206_2386+7207delinsGC
NM_175722.3:c.1891_1892delinsGC	NP_783653.1:p.Ala631=
XM_011510379.1:c.2386+7206_2386+7207delinsGC	XP_011508681.1:n.2386+7206_2386+7207delinsGC
XM_011510380.1:c.2410_2411delinsGC	XP_011508682.1:p.Ala804=
XM_011510381.1:c.2215+7206_2215+7207delinsGC	XP_011508683.1:n.2215+7206_2215+7207delinsGC
XR_922681.1:n.2411_2412delinsGC
XM_011510380.3:c.2446_2447delinsGC	XP_011508682.2:p.Ala816=
XM_024453085.1:c.2422+7206_2422+7207delinsGC	XP_024308853.1:n.2422+7206_2422+7207delinsGC
XM_024453086.1:c.2446_2447delinsGC	XP_024308854.1:p.Ala816=
XM_024453087.1:c.2386+7206_2386+7207delinsGC	XP_024308855.1:n.2386+7206_2386+7207delinsGC
XM_024453088.1:c.2386+7206_2386+7207delinsGC	XP_024308856.1:n.2386+7206_2386+7207delinsGC
XM_024453089.1:c.2386+7206_2386+7207delinsGC	XP_024308857.1:n.2386+7206_2386+7207delinsGC
XM_024453090.1:c.2422+7206_2422+7207delinsGC	XP_024308858.1:n.2422+7206_2422+7207delinsGC
XM_024453091.1:c.2275_2276delinsGC	XP_024308859.1:p.Ala759=
XM_024453092.1:c.2251+7206_2251+7207delinsGC	XP_024308860.1:n.2251+7206_2251+7207delinsGC
XM_024453093.1:c.1927_1928delinsGC	XP_024308861.1:p.Ala643=
NM_001206744.2:c.2410_2411delinsGC MANE Select	NP_001193673.1:p.Ala804=
NM_000547.6:c.2410_2411delinsGC	NP_000538.3:p.Ala804=
NM_001206745.2:c.2239_2240delinsGC	NP_001193674.1:p.Ala747=
NM_175719.4:c.2239_2240delinsGC	NP_783650.1:p.Ala747=