Canonical Allele Identifier: CA1511813

Gene: TPO

Linked Data

• dbSNP Id: rs773813701
• ExAC: 2:1491689 T / C
• gnomAD v2: 2-1491689-T-C
• gnomAD v4: 2-1487917-T-C
• MyVariant Identifiers: chr2:g.1491689T>C (hg19) ; chr2:g.1487917T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487917T>C , CM000664.2:g.1487917T>C	GRCh38
NC_000002.11:g.1491689T>C , CM000664.1:g.1491689T>C	GRCh37
NC_000002.10:g.1470696T>C	NCBI36
NG_011581.1:g.79455T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1694T>C MANE Select	ENSP00000329869.4:p.Phe565Ser
ENST00000329066.8:c.1694T>C	ENSP00000329869.4:p.Phe565Ser
ENST00000345913.8:c.1694T>C	ENSP00000318820.7:p.Phe565Ser
ENST00000346956.7:c.1694T>C	ENSP00000263886.6:p.Phe565Ser
ENST00000382198.5:c.1175T>C	ENSP00000371633.1:p.Phe392Ser
ENST00000382201.7:c.1597+3063T>C	ENSP00000371636.3:n.1597+3063T>C
ENST00000422464.5:c.1481T>C	ENSP00000405788.1:p.Phe494Ser
ENST00000446278.5:c.192+3063T>C
ENST00000462973.5:n.186+3063T>C
ENST00000469607.3:c.190+3063T>C	ENSP00000419461.1:n.190+3063T>C
ENST00000497517.6:n.439+3063T>C
NM_000547.5:c.1694T>C	NP_000538.3:p.Phe565Ser
NM_001206744.1:c.1694T>C	NP_001193673.1:p.Phe565Ser
NM_001206745.1:c.1597+3063T>C	NP_001193674.1:n.1597+3063T>C
NM_175719.3:c.1597+3063T>C	NP_783650.1:n.1597+3063T>C
NM_175721.3:c.1694T>C	NP_783652.1:p.Phe565Ser
NM_175722.3:c.1175T>C	NP_783653.1:p.Phe392Ser
XM_011510379.1:c.1694T>C	XP_011508681.1:p.Phe565Ser
XM_011510380.1:c.1694T>C	XP_011508682.1:p.Phe565Ser
XM_011510381.1:c.1597+3063T>C	XP_011508683.1:n.1597+3063T>C
XR_922681.1:n.1695T>C
XM_011510380.3:c.1730T>C	XP_011508682.2:p.Phe577Ser
XM_024453085.1:c.1730T>C	XP_024308853.1:p.Phe577Ser
XM_024453086.1:c.1730T>C	XP_024308854.1:p.Phe577Ser
XM_024453087.1:c.1694T>C	XP_024308855.1:p.Phe565Ser
XM_024453088.1:c.1694T>C	XP_024308856.1:p.Phe565Ser
XM_024453089.1:c.1694T>C	XP_024308857.1:p.Phe565Ser
XM_024453090.1:c.1730T>C	XP_024308858.1:p.Phe577Ser
XM_024453091.1:c.1633+3063T>C	XP_024308859.1:n.1633+3063T>C
XM_024453092.1:c.1633+3063T>C	XP_024308860.1:n.1633+3063T>C
XM_024453093.1:c.1211T>C	XP_024308861.1:p.Phe404Ser
NM_001206744.2:c.1694T>C MANE Select	NP_001193673.1:p.Phe565Ser
NM_000547.6:c.1694T>C	NP_000538.3:p.Phe565Ser
NM_001206745.2:c.1597+3063T>C	NP_001193674.1:n.1597+3063T>C
NM_175719.4:c.1597+3063T>C	NP_783650.1:n.1597+3063T>C