Canonical Allele Identifier: CA1511963

Gene: TPO

Linked Data

• dbSNP Id: rs775227003
• ExAC: 2:1499905 C / G
• gnomAD v2: 2-1499905-C-G
• gnomAD v4: 2-1496133-C-G
• MyVariant Identifiers: chr2:g.1499905C>G (hg19) ; chr2:g.1496133C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1496133C>G , CM000664.2:g.1496133C>G	GRCh38
NC_000002.11:g.1499905C>G , CM000664.1:g.1499905C>G	GRCh37
NC_000002.10:g.1478912C>G	NCBI36
NG_011581.1:g.87671C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2151C>G MANE Select	ENSP00000329869.4:p.Asp717Glu
ENST00000329066.8:c.2151C>G	ENSP00000329869.4:p.Asp717Glu
ENST00000345913.8:c.2151C>G	ENSP00000318820.7:p.Asp717Glu
ENST00000346956.7:c.2151C>G	ENSP00000263886.6:p.Asp717Glu
ENST00000382198.5:c.1632C>G	ENSP00000371633.1:p.Asp544Glu
ENST00000382201.7:c.1980C>G	ENSP00000371636.3:p.Asp660Glu
ENST00000422464.5:c.1938C>G	ENSP00000405788.1:p.Asp646Glu
ENST00000446278.5:c.575C>G
ENST00000462973.5:n.424+2094C>G
ENST00000469607.3:c.573C>G	ENSP00000419461.1:p.Asp191Glu
ENST00000497517.6:n.677+2094C>G
NM_000547.5:c.2151C>G	NP_000538.3:p.Asp717Glu
NM_001206744.1:c.2151C>G	NP_001193673.1:p.Asp717Glu
NM_001206745.1:c.1980C>G	NP_001193674.1:p.Asp660Glu
NM_175719.3:c.1980C>G	NP_783650.1:p.Asp660Glu
NM_175721.3:c.2151C>G	NP_783652.1:p.Asp717Glu
NM_175722.3:c.1632C>G	NP_783653.1:p.Asp544Glu
XM_011510379.1:c.2151C>G	XP_011508681.1:p.Asp717Glu
XM_011510380.1:c.2151C>G	XP_011508682.1:p.Asp717Glu
XM_011510381.1:c.1980C>G	XP_011508683.1:p.Asp660Glu
XR_922681.1:n.2152C>G
XM_011510380.3:c.2187C>G	XP_011508682.2:p.Asp729Glu
XM_024453085.1:c.2187C>G	XP_024308853.1:p.Asp729Glu
XM_024453086.1:c.2187C>G	XP_024308854.1:p.Asp729Glu
XM_024453087.1:c.2151C>G	XP_024308855.1:p.Asp717Glu
XM_024453088.1:c.2151C>G	XP_024308856.1:p.Asp717Glu
XM_024453089.1:c.2151C>G	XP_024308857.1:p.Asp717Glu
XM_024453090.1:c.2187C>G	XP_024308858.1:p.Asp729Glu
XM_024453091.1:c.2016C>G	XP_024308859.1:p.Asp672Glu
XM_024453092.1:c.2016C>G	XP_024308860.1:p.Asp672Glu
XM_024453093.1:c.1668C>G	XP_024308861.1:p.Asp556Glu
NM_001206744.2:c.2151C>G MANE Select	NP_001193673.1:p.Asp717Glu
NM_000547.6:c.2151C>G	NP_000538.3:p.Asp717Glu
NM_001206745.2:c.1980C>G	NP_001193674.1:p.Asp660Glu
NM_175719.4:c.1980C>G	NP_783650.1:p.Asp660Glu