Canonical Allele Identifier: CA424757117
Gene: TPO HGNC NCBI

Linked Data

gnomAD v4: 2-1496154-C-T
MyVariant Identifiers: chr2:g.1499926C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1496154C>T , CM000664.2:g.1496154C>T GRCh38
NC_000002.11:g.1499926C>T , CM000664.1:g.1499926C>T GRCh37
NC_000002.10:g.1478933C>T NCBI36
NG_011581.1:g.87692C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329066.9:c.2172C>T MANE Select ENSP00000329869.4:p.Ile724=
ENST00000329066.8:c.2172C>T ENSP00000329869.4:p.Ile724=
ENST00000345913.8:c.2172C>T ENSP00000318820.7:p.Ile724=
ENST00000346956.7:c.2172C>T ENSP00000263886.6:p.Ile724=
ENST00000382198.5:c.1653C>T ENSP00000371633.1:p.Ile551=
ENST00000382201.7:c.2001C>T ENSP00000371636.3:p.Ile667=
ENST00000422464.5:c.1959C>T ENSP00000405788.1:p.Ile653=
ENST00000446278.5:c.596C>T
ENST00000462973.5:n.424+2115C>T
ENST00000469607.3:c.594C>T ENSP00000419461.1:p.Ile198=
ENST00000497517.6:n.677+2115C>T
NM_000547.5:c.2172C>T NP_000538.3:p.Ile724=
NM_001206744.1:c.2172C>T NP_001193673.1:p.Ile724=
NM_001206745.1:c.2001C>T NP_001193674.1:p.Ile667=
NM_175719.3:c.2001C>T NP_783650.1:p.Ile667=
NM_175721.3:c.2172C>T NP_783652.1:p.Ile724=
NM_175722.3:c.1653C>T NP_783653.1:p.Ile551=
XM_011510379.1:c.2172C>T XP_011508681.1:p.Ile724=
XM_011510380.1:c.2172C>T XP_011508682.1:p.Ile724=
XM_011510381.1:c.2001C>T XP_011508683.1:p.Ile667=
XR_922681.1:n.2173C>T
XM_011510380.3:c.2208C>T XP_011508682.2:p.Ile736=
XM_024453085.1:c.2208C>T XP_024308853.1:p.Ile736=
XM_024453086.1:c.2208C>T XP_024308854.1:p.Ile736=
XM_024453087.1:c.2172C>T XP_024308855.1:p.Ile724=
XM_024453088.1:c.2172C>T XP_024308856.1:p.Ile724=
XM_024453089.1:c.2172C>T XP_024308857.1:p.Ile724=
XM_024453090.1:c.2208C>T XP_024308858.1:p.Ile736=
XM_024453091.1:c.2037C>T XP_024308859.1:p.Ile679=
XM_024453092.1:c.2037C>T XP_024308860.1:p.Ile679=
XM_024453093.1:c.1689C>T XP_024308861.1:p.Ile563=
NM_001206744.2:c.2172C>T MANE Select NP_001193673.1:p.Ile724=
NM_000547.6:c.2172C>T NP_000538.3:p.Ile724=
NM_001206745.2:c.2001C>T NP_001193674.1:p.Ile667=
NM_175719.4:c.2001C>T NP_783650.1:p.Ile667=