Canonical Allele Identifier: CA1233577778

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1495873_1495874delinsTG , CM000664.2:g.1495873_1495874delinsTG	GRCh38
NC_000002.11:g.1499645_1499646delinsTG , CM000664.1:g.1499645_1499646delinsTG	GRCh37
NC_000002.10:g.1478652_1478653delinsTG	NCBI36
NG_011581.1:g.87411_87412delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2007-116_2007-115delinsTG MANE Select	ENSP00000329869.4:n.2007-116_2007-115delinsTG
ENST00000329066.8:c.2007-116_2007-115delinsTG	ENSP00000329869.4:n.2007-116_2007-115delinsTG
ENST00000345913.8:c.2007-116_2007-115delinsTG	ENSP00000318820.7:n.2007-116_2007-115delinsTG
ENST00000346956.7:c.2007-116_2007-115delinsTG	ENSP00000263886.6:n.2007-116_2007-115delinsTG
ENST00000382198.5:c.1488-116_1488-115delinsTG	ENSP00000371633.1:n.1488-116_1488-115delinsTG
ENST00000382201.7:c.1836-116_1836-115delinsTG	ENSP00000371636.3:n.1836-116_1836-115delinsTG
ENST00000422464.5:c.1794-116_1794-115delinsTG	ENSP00000405788.1:n.1794-116_1794-115delinsTG
ENST00000446278.5:c.431-116_431-115delinsTG
ENST00000462973.5:n.424+1834_424+1835delinsTG
ENST00000469607.3:c.429-116_429-115delinsTG	ENSP00000419461.1:n.429-116_429-115delinsTG
ENST00000497517.6:n.677+1834_677+1835delinsTG
NM_000547.5:c.2007-116_2007-115delinsTG	NP_000538.3:n.2007-116_2007-115delinsTG
NM_001206744.1:c.2007-116_2007-115delinsTG	NP_001193673.1:n.2007-116_2007-115delinsTG
NM_001206745.1:c.1836-116_1836-115delinsTG	NP_001193674.1:n.1836-116_1836-115delinsTG
NM_175719.3:c.1836-116_1836-115delinsTG	NP_783650.1:n.1836-116_1836-115delinsTG
NM_175721.3:c.2007-116_2007-115delinsTG	NP_783652.1:n.2007-116_2007-115delinsTG
NM_175722.3:c.1488-116_1488-115delinsTG	NP_783653.1:n.1488-116_1488-115delinsTG
XM_011510379.1:c.2007-116_2007-115delinsTG	XP_011508681.1:n.2007-116_2007-115delinsTG
XM_011510380.1:c.2007-116_2007-115delinsTG	XP_011508682.1:n.2007-116_2007-115delinsTG
XM_011510381.1:c.1836-116_1836-115delinsTG	XP_011508683.1:n.1836-116_1836-115delinsTG
XR_922681.1:n.2008-116_2008-115delinsTG
XM_011510380.3:c.2043-116_2043-115delinsTG	XP_011508682.2:n.2043-116_2043-115delinsTG
XM_024453085.1:c.2043-116_2043-115delinsTG	XP_024308853.1:n.2043-116_2043-115delinsTG
XM_024453086.1:c.2043-116_2043-115delinsTG	XP_024308854.1:n.2043-116_2043-115delinsTG
XM_024453087.1:c.2007-116_2007-115delinsTG	XP_024308855.1:n.2007-116_2007-115delinsTG
XM_024453088.1:c.2007-116_2007-115delinsTG	XP_024308856.1:n.2007-116_2007-115delinsTG
XM_024453089.1:c.2007-116_2007-115delinsTG	XP_024308857.1:n.2007-116_2007-115delinsTG
XM_024453090.1:c.2043-116_2043-115delinsTG	XP_024308858.1:n.2043-116_2043-115delinsTG
XM_024453091.1:c.1872-116_1872-115delinsTG	XP_024308859.1:n.1872-116_1872-115delinsTG
XM_024453092.1:c.1872-116_1872-115delinsTG	XP_024308860.1:n.1872-116_1872-115delinsTG
XM_024453093.1:c.1524-116_1524-115delinsTG	XP_024308861.1:n.1524-116_1524-115delinsTG
NM_001206744.2:c.2007-116_2007-115delinsTG MANE Select	NP_001193673.1:n.2007-116_2007-115delinsTG
NM_000547.6:c.2007-116_2007-115delinsTG	NP_000538.3:n.2007-116_2007-115delinsTG
NM_001206745.2:c.1836-116_1836-115delinsTG	NP_001193674.1:n.1836-116_1836-115delinsTG
NM_175719.4:c.1836-116_1836-115delinsTG	NP_783650.1:n.1836-116_1836-115delinsTG