Canonical Allele Identifier: CA424502956

Gene: TPO

Linked Data

• dbSNP Id: rs1558343989
• MyVariant Identifiers: chr2:g.1488391C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1484619C>T , CM000664.2:g.1484619C>T	GRCh38
NC_000002.11:g.1488391C>T , CM000664.1:g.1488391C>T	GRCh37
NC_000002.10:g.1467398C>T	NCBI36
NG_011581.1:g.76157C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000329066.9:c.1362C>T MANE Select	ENSP00000329869.4:p.Ile454=
ENST00000329066.8:c.1362C>T	ENSP00000329869.4:p.Ile454=
ENST00000345913.8:c.1362C>T	ENSP00000318820.7:p.Ile454=
ENST00000346956.7:c.1362C>T	ENSP00000263886.6:p.Ile454=
ENST00000382198.5:c.843C>T	ENSP00000371633.1:p.Ile281=
ENST00000382201.7:c.1362C>T	ENSP00000371636.3:p.Ile454=
ENST00000422464.5:c.1149C>T	ENSP00000405788.1:p.Ile383=
ENST00000497517.6:n.204C>T
NM_000547.5:c.1362C>T	NP_000538.3:p.Ile454=
NM_001206744.1:c.1362C>T	NP_001193673.1:p.Ile454=
NM_001206745.1:c.1362C>T	NP_001193674.1:p.Ile454=
NM_175719.3:c.1362C>T	NP_783650.1:p.Ile454=
NM_175721.3:c.1362C>T	NP_783652.1:p.Ile454=
NM_175722.3:c.843C>T	NP_783653.1:p.Ile281=
XM_011510379.1:c.1362C>T	XP_011508681.1:p.Ile454=
XM_011510380.1:c.1362C>T	XP_011508682.1:p.Ile454=
XM_011510381.1:c.1362C>T	XP_011508683.1:p.Ile454=
XR_922681.1:n.1363C>T
XM_011510380.3:c.1398C>T	XP_011508682.2:p.Ile466=
XM_024453085.1:c.1398C>T	XP_024308853.1:p.Ile466=
XM_024453086.1:c.1398C>T	XP_024308854.1:p.Ile466=
XM_024453087.1:c.1362C>T	XP_024308855.1:p.Ile454=
XM_024453088.1:c.1362C>T	XP_024308856.1:p.Ile454=
XM_024453089.1:c.1362C>T	XP_024308857.1:p.Ile454=
XM_024453090.1:c.1398C>T	XP_024308858.1:p.Ile466=
XM_024453091.1:c.1398C>T	XP_024308859.1:p.Ile466=
XM_024453092.1:c.1398C>T	XP_024308860.1:p.Ile466=
XM_024453093.1:c.879C>T	XP_024308861.1:p.Ile293=
NM_001206744.2:c.1362C>T MANE Select	NP_001193673.1:p.Ile454=
NM_000547.6:c.1362C>T	NP_000538.3:p.Ile454=
NM_001206745.2:c.1362C>T	NP_001193674.1:p.Ile454=
NM_175719.4:c.1362C>T	NP_783650.1:p.Ile454=