Canonical Allele Identifier: CA2698748540

Gene: TPO

Linked Data

• dbSNP Id: rs2148673397

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1477443_1477446del , CM000664.2:g.1477443_1477446del	GRCh38
NC_000002.11:g.1481215_1481218del , CM000664.1:g.1481215_1481218del	GRCh37
NC_000002.10:g.1460222_1460225del	NCBI36
NG_011581.1:g.68981_68984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1177_1180del MANE Select	ENSP00000329869.4:p.Gly393ThrfsTer10
ENST00000329066.8:c.1177_1180del	ENSP00000329869.4:p.Gly393ThrfsTer10
ENST00000345913.8:c.1177_1180del	ENSP00000318820.7:p.Gly393ThrfsTer10
ENST00000346956.7:c.1177_1180del	ENSP00000263886.6:p.Gly393ThrfsTer10
ENST00000382198.5:c.820-7153_820-7150del	ENSP00000371633.1:n.820-7153_820-7150del
ENST00000382201.7:c.1177_1180del	ENSP00000371636.3:p.Gly393ThrfsTer10
ENST00000422464.5:c.964_967del	ENSP00000405788.1:p.Gly322ThrfsTer10
ENST00000497517.6:n.181-7153_181-7150del
NM_000547.5:c.1177_1180del	NP_000538.3:p.Gly393ThrfsTer10
NM_001206744.1:c.1177_1180del	NP_001193673.1:p.Gly393ThrfsTer10
NM_001206745.1:c.1177_1180del	NP_001193674.1:p.Gly393ThrfsTer10
NM_175719.3:c.1177_1180del	NP_783650.1:p.Gly393ThrfsTer10
NM_175721.3:c.1177_1180del	NP_783652.1:p.Gly393ThrfsTer10
NM_175722.3:c.820-7153_820-7150del	NP_783653.1:n.820-7153_820-7150del
XM_011510379.1:c.1177_1180del	XP_011508681.1:p.Gly393ThrfsTer10
XM_011510380.1:c.1177_1180del	XP_011508682.1:p.Gly393ThrfsTer10
XM_011510381.1:c.1177_1180del	XP_011508683.1:p.Gly393ThrfsTer10
XM_011510382.1:c.1177_1180del	XP_011508684.1:p.Gly393ThrfsTer10
XR_922681.1:n.1178_1181del
XM_011510380.3:c.1213_1216del	XP_011508682.2:p.Gly405ThrfsTer10
XM_024453085.1:c.1213_1216del	XP_024308853.1:p.Gly405ThrfsTer10
XM_024453086.1:c.1213_1216del	XP_024308854.1:p.Gly405ThrfsTer10
XM_024453087.1:c.1177_1180del	XP_024308855.1:p.Gly393ThrfsTer10
XM_024453088.1:c.1177_1180del	XP_024308856.1:p.Gly393ThrfsTer10
XM_024453089.1:c.1177_1180del	XP_024308857.1:p.Gly393ThrfsTer10
XM_024453090.1:c.1213_1216del	XP_024308858.1:p.Gly405ThrfsTer10
XM_024453091.1:c.1213_1216del	XP_024308859.1:p.Gly405ThrfsTer10
XM_024453092.1:c.1213_1216del	XP_024308860.1:p.Gly405ThrfsTer10
XM_024453093.1:c.856-7153_856-7150del	XP_024308861.1:n.856-7153_856-7150del
NM_001206744.2:c.1177_1180del MANE Select	NP_001193673.1:p.Gly393ThrfsTer10
NM_000547.6:c.1177_1180del	NP_000538.3:p.Gly393ThrfsTer10
NM_001206745.2:c.1177_1180del	NP_001193674.1:p.Gly393ThrfsTer10
NM_175719.4:c.1177_1180del	NP_783650.1:p.Gly393ThrfsTer10