Canonical Allele Identifier: CA1233581679
Gene: TPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1503955C= , CM000664.2:g.1503955C= GRCh38
NC_000002.11:g.1507727C= , CM000664.1:g.1507727C= GRCh37
NC_000002.10:g.1486734C= NCBI36
NG_011581.1:g.95493C=

Transcript Alleles

HGVS Amino-acid Change
NM_001206744.2:c.2394C= MANE Select NP_001193673.1:p.Asn798=
ENST00000329066.9:c.2394C= MANE Select ENSP00000329869.4:p.Asn798=
NM_000547.5:c.2394C= NP_000538.3:p.Asn798=
NM_000547.6:c.2394C= NP_000538.3:p.Asn798=
NM_001206744.1:c.2394C= NP_001193673.1:p.Asn798=
NM_001206745.1:c.2223C= NP_001193674.1:p.Asn741=
NM_001206745.2:c.2223C= NP_001193674.1:p.Asn741=
NM_175719.3:c.2223C= NP_783650.1:p.Asn741=
NM_175719.4:c.2223C= NP_783650.1:p.Asn741=
NM_175721.3:c.2386+7190C= NP_783652.1:n.2386+7190C=
NM_175722.3:c.1875C= NP_783653.1:p.Asn625=
ENST00000329066.8:c.2394C= ENSP00000329869.4:p.Asn798=
ENST00000345913.8:c.2394C= ENSP00000318820.7:p.Asn798=
ENST00000346956.7:c.2386+7190C= ENSP00000263886.6:n.2386+7190C=
ENST00000382198.5:c.1875C= ENSP00000371633.1:p.Asn625=
ENST00000382201.7:c.2223C= ENSP00000371636.3:p.Asn741=
ENST00000422464.5:c.2173+7190C= ENSP00000405788.1:n.2173+7190C=
ENST00000425083.3:n.57C=
ENST00000446278.5:c.818C=
ENST00000462973.5:n.424+9916C=
ENST00000469607.3:c.808+7190C= ENSP00000419461.1:n.808+7190C=
ENST00000497517.6:n.685C=
XM_011510379.1:c.2386+7190C= XP_011508681.1:n.2386+7190C=
XM_011510380.1:c.2394C= XP_011508682.1:p.Asn798=
XM_011510380.3:c.2430C= XP_011508682.2:p.Asn810=
XM_011510381.1:c.2215+7190C= XP_011508683.1:n.2215+7190C=
XM_024453085.1:c.2422+7190C= XP_024308853.1:n.2422+7190C=
XM_024453086.1:c.2430C= XP_024308854.1:p.Asn810=
XM_024453087.1:c.2386+7190C= XP_024308855.1:n.2386+7190C=
XM_024453088.1:c.2386+7190C= XP_024308856.1:n.2386+7190C=
XM_024453089.1:c.2386+7190C= XP_024308857.1:n.2386+7190C=
XM_024453090.1:c.2422+7190C= XP_024308858.1:n.2422+7190C=
XM_024453091.1:c.2259C= XP_024308859.1:p.Asn753=
XM_024453092.1:c.2251+7190C= XP_024308860.1:n.2251+7190C=
XM_024453093.1:c.1911C= XP_024308861.1:p.Asn637=
XR_922681.1:n.2395C=