Canonical Allele Identifier: CA345694351
Gene: TPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1477336G>C , CM000664.2:g.1477336G>C GRCh38
NC_000002.11:g.1481108G>C , CM000664.1:g.1481108G>C GRCh37
NC_000002.10:g.1460115G>C NCBI36
NG_011581.1:g.68874G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329066.9:c.1070G>C MANE Select ENSP00000329869.4:p.Arg357Pro
ENST00000329066.8:c.1070G>C ENSP00000329869.4:p.Arg357Pro
ENST00000345913.8:c.1070G>C ENSP00000318820.7:p.Arg357Pro
ENST00000346956.7:c.1070G>C ENSP00000263886.6:p.Arg357Pro
ENST00000382198.5:c.820-7260G>C ENSP00000371633.1:n.820-7260G>C
ENST00000382201.7:c.1070G>C ENSP00000371636.3:p.Arg357Pro
ENST00000422464.5:c.857G>C ENSP00000405788.1:p.Arg286Pro
ENST00000497517.6:n.181-7260G>C
NM_000547.5:c.1070G>C NP_000538.3:p.Arg357Pro
NM_001206744.1:c.1070G>C NP_001193673.1:p.Arg357Pro
NM_001206745.1:c.1070G>C NP_001193674.1:p.Arg357Pro
NM_175719.3:c.1070G>C NP_783650.1:p.Arg357Pro
NM_175721.3:c.1070G>C NP_783652.1:p.Arg357Pro
NM_175722.3:c.820-7260G>C NP_783653.1:n.820-7260G>C
XM_011510379.1:c.1070G>C XP_011508681.1:p.Arg357Pro
XM_011510380.1:c.1070G>C XP_011508682.1:p.Arg357Pro
XM_011510381.1:c.1070G>C XP_011508683.1:p.Arg357Pro
XM_011510382.1:c.1070G>C XP_011508684.1:p.Arg357Pro
XR_922681.1:n.1071G>C
XM_011510380.3:c.1106G>C XP_011508682.2:p.Arg369Pro
XM_024453085.1:c.1106G>C XP_024308853.1:p.Arg369Pro
XM_024453086.1:c.1106G>C XP_024308854.1:p.Arg369Pro
XM_024453087.1:c.1070G>C XP_024308855.1:p.Arg357Pro
XM_024453088.1:c.1070G>C XP_024308856.1:p.Arg357Pro
XM_024453089.1:c.1070G>C XP_024308857.1:p.Arg357Pro
XM_024453090.1:c.1106G>C XP_024308858.1:p.Arg369Pro
XM_024453091.1:c.1106G>C XP_024308859.1:p.Arg369Pro
XM_024453092.1:c.1106G>C XP_024308860.1:p.Arg369Pro
XM_024453093.1:c.856-7260G>C XP_024308861.1:n.856-7260G>C
NM_001206744.2:c.1070G>C MANE Select NP_001193673.1:p.Arg357Pro
NM_000547.6:c.1070G>C NP_000538.3:p.Arg357Pro
NM_001206745.2:c.1070G>C NP_001193674.1:p.Arg357Pro
NM_175719.4:c.1070G>C NP_783650.1:p.Arg357Pro