Canonical Allele Identifier: CA116630
Gene: TPO HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 4044
dbSNP Id: rs121908083

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1484614T>G , CM000664.2:g.1484614T>G GRCh38
NC_000002.10:g.1467393T>G NCBI36
NC_000002.11:g.1488386T>G , CM000664.1:g.1488386T>G GRCh37
NG_011581.1:g.76152T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000329066.8:c.1357T>G ENSP00000329869.4:p.Tyr453Asp
ENST00000345913.8:c.1357T>G ENSP00000318820.7:p.Tyr453Asp
ENST00000346956.7:c.1357T>G ENSP00000263886.6:p.Tyr453Asp
ENST00000382198.5:n.838T>G ENSP00000371633.1:p.Tyr280Asp
ENST00000382201.7:c.1357T>G ENSP00000371636.3:p.Tyr453Asp
ENST00000422464.5:n.1144T>G ENSP00000405788.1:p.Tyr382Asp
ENST00000497517.6:n.199T>G
NM_000547.5:c.1357T>G VV NP_000538.3:p.Tyr453Asp
NM_001206744.1:c.1357T>G VV NP_001193673.1:p.Tyr453Asp
NM_001206745.1:c.1357T>G VV NP_001193674.1:p.Tyr453Asp
NM_175719.3:c.1357T>G VV NP_783650.1:p.Tyr453Asp
NM_175721.3:c.1357T>G VV NP_783652.1:p.Tyr453Asp
NM_175722.3:c.838T>G VV NP_783653.1:p.Tyr280Asp
XM_011510379.1:c.1357T>G XP_011508681.1:p.Tyr453Asp
XM_011510380.1:c.1357T>G XP_011508682.1:p.Tyr453Asp
XM_011510381.1:c.1357T>G XP_011508683.1:p.Tyr453Asp
XR_922681.1:n.1358T>G
XM_011510380.3:c.1393T>G XP_011508682.2:p.Tyr465Asp
XM_024453085.1:c.1393T>G XP_024308853.1:p.Tyr465Asp
XM_024453086.1:c.1393T>G XP_024308854.1:p.Tyr465Asp
XM_024453087.1:c.1357T>G XP_024308855.1:p.Tyr453Asp
XM_024453088.1:c.1357T>G XP_024308856.1:p.Tyr453Asp
XM_024453089.1:c.1357T>G XP_024308857.1:p.Tyr453Asp
XM_024453090.1:c.1393T>G XP_024308858.1:p.Tyr465Asp
XM_024453091.1:c.1393T>G XP_024308859.1:p.Tyr465Asp
XM_024453092.1:c.1393T>G XP_024308860.1:p.Tyr465Asp
XM_024453093.1:c.874T>G XP_024308861.1:p.Tyr292Asp