Canonical Allele Identifier: CA1233577741

Gene: TPO

Linked Data

• dbSNP Id: rs1672268950

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1495814_1495815insG , CM000664.2:g.1495814_1495815insG	GRCh38
NC_000002.11:g.1499586_1499587insG , CM000664.1:g.1499586_1499587insG	GRCh37
NC_000002.10:g.1478593_1478594insG	NCBI36
NG_011581.1:g.87352_87353insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2007-175_2007-174insG MANE Select	ENSP00000329869.4:n.2007-175_2007-174insG
ENST00000329066.8:c.2007-175_2007-174insG	ENSP00000329869.4:n.2007-175_2007-174insG
ENST00000345913.8:c.2007-175_2007-174insG	ENSP00000318820.7:n.2007-175_2007-174insG
ENST00000346956.7:c.2007-175_2007-174insG	ENSP00000263886.6:n.2007-175_2007-174insG
ENST00000382198.5:c.1488-175_1488-174insG	ENSP00000371633.1:n.1488-175_1488-174insG
ENST00000382201.7:c.1836-175_1836-174insG	ENSP00000371636.3:n.1836-175_1836-174insG
ENST00000422464.5:c.1794-175_1794-174insG	ENSP00000405788.1:n.1794-175_1794-174insG
ENST00000446278.5:c.431-175_431-174insG
ENST00000462973.5:n.424+1775_424+1776insG
ENST00000469607.3:c.429-175_429-174insG	ENSP00000419461.1:n.429-175_429-174insG
ENST00000497517.6:n.677+1775_677+1776insG
NM_000547.5:c.2007-175_2007-174insG	NP_000538.3:n.2007-175_2007-174insG
NM_001206744.1:c.2007-175_2007-174insG	NP_001193673.1:n.2007-175_2007-174insG
NM_001206745.1:c.1836-175_1836-174insG	NP_001193674.1:n.1836-175_1836-174insG
NM_175719.3:c.1836-175_1836-174insG	NP_783650.1:n.1836-175_1836-174insG
NM_175721.3:c.2007-175_2007-174insG	NP_783652.1:n.2007-175_2007-174insG
NM_175722.3:c.1488-175_1488-174insG	NP_783653.1:n.1488-175_1488-174insG
XM_011510379.1:c.2007-175_2007-174insG	XP_011508681.1:n.2007-175_2007-174insG
XM_011510380.1:c.2007-175_2007-174insG	XP_011508682.1:n.2007-175_2007-174insG
XM_011510381.1:c.1836-175_1836-174insG	XP_011508683.1:n.1836-175_1836-174insG
XR_922681.1:n.2008-175_2008-174insG
XM_011510380.3:c.2043-175_2043-174insG	XP_011508682.2:n.2043-175_2043-174insG
XM_024453085.1:c.2043-175_2043-174insG	XP_024308853.1:n.2043-175_2043-174insG
XM_024453086.1:c.2043-175_2043-174insG	XP_024308854.1:n.2043-175_2043-174insG
XM_024453087.1:c.2007-175_2007-174insG	XP_024308855.1:n.2007-175_2007-174insG
XM_024453088.1:c.2007-175_2007-174insG	XP_024308856.1:n.2007-175_2007-174insG
XM_024453089.1:c.2007-175_2007-174insG	XP_024308857.1:n.2007-175_2007-174insG
XM_024453090.1:c.2043-175_2043-174insG	XP_024308858.1:n.2043-175_2043-174insG
XM_024453091.1:c.1872-175_1872-174insG	XP_024308859.1:n.1872-175_1872-174insG
XM_024453092.1:c.1872-175_1872-174insG	XP_024308860.1:n.1872-175_1872-174insG
XM_024453093.1:c.1524-175_1524-174insG	XP_024308861.1:n.1524-175_1524-174insG
NM_001206744.2:c.2007-175_2007-174insG MANE Select	NP_001193673.1:n.2007-175_2007-174insG
NM_000547.6:c.2007-175_2007-174insG	NP_000538.3:n.2007-175_2007-174insG
NM_001206745.2:c.1836-175_1836-174insG	NP_001193674.1:n.1836-175_1836-174insG
NM_175719.4:c.1836-175_1836-174insG	NP_783650.1:n.1836-175_1836-174insG