Canonical Allele Identifier: CA2657645888
Gene: TPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1477219_1477220del , CM000664.2:g.1477219_1477220del GRCh38
NC_000002.11:g.1480991_1480992del , CM000664.1:g.1480991_1480992del GRCh37
NC_000002.10:g.1459998_1459999del NCBI36
NG_011581.1:g.68757_68758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000329066.9:c.953_954del MANE Select ENSP00000329869.4:p.Asn318ArgfsTer?
ENST00000329066.8:c.953_954del ENSP00000329869.4:p.Asn318ArgfsTer?
ENST00000345913.8:c.953_954del ENSP00000318820.7:p.Asn318ArgfsTer?
ENST00000346956.7:c.953_954del ENSP00000263886.6:p.Asn318ArgfsTer?
ENST00000382198.5:c.820-7377_820-7376del ENSP00000371633.1:n.820-7377_820-7376del
ENST00000382201.7:c.953_954del ENSP00000371636.3:p.Asn318ArgfsTer?
ENST00000422464.5:c.740_741del ENSP00000405788.1:p.Asn247ArgfsTer?
ENST00000497517.6:n.181-7377_181-7376del
NM_000547.5:c.953_954del NP_000538.3:p.Asn318ArgfsTer?
NM_001206744.1:c.953_954del NP_001193673.1:p.Asn318ArgfsTer?
NM_001206745.1:c.953_954del NP_001193674.1:p.Asn318ArgfsTer?
NM_175719.3:c.953_954del NP_783650.1:p.Asn318ArgfsTer?
NM_175721.3:c.953_954del NP_783652.1:p.Asn318ArgfsTer?
NM_175722.3:c.820-7377_820-7376del NP_783653.1:n.820-7377_820-7376del
XM_011510379.1:c.953_954del XP_011508681.1:p.Asn318ArgfsTer?
XM_011510380.1:c.953_954del XP_011508682.1:p.Asn318ArgfsTer?
XM_011510381.1:c.953_954del XP_011508683.1:p.Asn318ArgfsTer?
XM_011510382.1:c.953_954del XP_011508684.1:p.Asn318ArgfsTer?
XR_922681.1:n.954_955del
XM_011510380.3:c.989_990del XP_011508682.2:p.Asn330ArgfsTer?
XM_024453085.1:c.989_990del XP_024308853.1:p.Asn330ArgfsTer?
XM_024453086.1:c.989_990del XP_024308854.1:p.Asn330ArgfsTer?
XM_024453087.1:c.953_954del XP_024308855.1:p.Asn318ArgfsTer?
XM_024453088.1:c.953_954del XP_024308856.1:p.Asn318ArgfsTer?
XM_024453089.1:c.953_954del XP_024308857.1:p.Asn318ArgfsTer?
XM_024453090.1:c.989_990del XP_024308858.1:p.Asn330ArgfsTer?
XM_024453091.1:c.989_990del XP_024308859.1:p.Asn330ArgfsTer?
XM_024453092.1:c.989_990del XP_024308860.1:p.Asn330ArgfsTer?
XM_024453093.1:c.856-7377_856-7376del XP_024308861.1:n.856-7377_856-7376del
NM_001206744.2:c.953_954del MANE Select NP_001193673.1:p.Asn318ArgfsTer?
NM_000547.6:c.953_954del NP_000538.3:p.Asn318ArgfsTer?
NM_001206745.2:c.953_954del NP_001193674.1:p.Asn318ArgfsTer?
NM_175719.4:c.953_954del NP_783650.1:p.Asn318ArgfsTer?