Canonical Allele Identifier: CA1233577816

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1495939_1495940delinsTG , CM000664.2:g.1495939_1495940delinsTG	GRCh38
NC_000002.11:g.1499711_1499712delinsTG , CM000664.1:g.1499711_1499712delinsTG	GRCh37
NC_000002.10:g.1478718_1478719delinsTG	NCBI36
NG_011581.1:g.87477_87478delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2007-50_2007-49delinsTG MANE Select	ENSP00000329869.4:n.2007-50_2007-49delinsTG
ENST00000329066.8:c.2007-50_2007-49delinsTG	ENSP00000329869.4:n.2007-50_2007-49delinsTG
ENST00000345913.8:c.2007-50_2007-49delinsTG	ENSP00000318820.7:n.2007-50_2007-49delinsTG
ENST00000346956.7:c.2007-50_2007-49delinsTG	ENSP00000263886.6:n.2007-50_2007-49delinsTG
ENST00000382198.5:c.1488-50_1488-49delinsTG	ENSP00000371633.1:n.1488-50_1488-49delinsTG
ENST00000382201.7:c.1836-50_1836-49delinsTG	ENSP00000371636.3:n.1836-50_1836-49delinsTG
ENST00000422464.5:c.1794-50_1794-49delinsTG	ENSP00000405788.1:n.1794-50_1794-49delinsTG
ENST00000446278.5:c.431-50_431-49delinsTG
ENST00000462973.5:n.424+1900_424+1901delinsTG
ENST00000469607.3:c.429-50_429-49delinsTG	ENSP00000419461.1:n.429-50_429-49delinsTG
ENST00000497517.6:n.677+1900_677+1901delinsTG
NM_000547.5:c.2007-50_2007-49delinsTG	NP_000538.3:n.2007-50_2007-49delinsTG
NM_001206744.1:c.2007-50_2007-49delinsTG	NP_001193673.1:n.2007-50_2007-49delinsTG
NM_001206745.1:c.1836-50_1836-49delinsTG	NP_001193674.1:n.1836-50_1836-49delinsTG
NM_175719.3:c.1836-50_1836-49delinsTG	NP_783650.1:n.1836-50_1836-49delinsTG
NM_175721.3:c.2007-50_2007-49delinsTG	NP_783652.1:n.2007-50_2007-49delinsTG
NM_175722.3:c.1488-50_1488-49delinsTG	NP_783653.1:n.1488-50_1488-49delinsTG
XM_011510379.1:c.2007-50_2007-49delinsTG	XP_011508681.1:n.2007-50_2007-49delinsTG
XM_011510380.1:c.2007-50_2007-49delinsTG	XP_011508682.1:n.2007-50_2007-49delinsTG
XM_011510381.1:c.1836-50_1836-49delinsTG	XP_011508683.1:n.1836-50_1836-49delinsTG
XR_922681.1:n.2008-50_2008-49delinsTG
XM_011510380.3:c.2043-50_2043-49delinsTG	XP_011508682.2:n.2043-50_2043-49delinsTG
XM_024453085.1:c.2043-50_2043-49delinsTG	XP_024308853.1:n.2043-50_2043-49delinsTG
XM_024453086.1:c.2043-50_2043-49delinsTG	XP_024308854.1:n.2043-50_2043-49delinsTG
XM_024453087.1:c.2007-50_2007-49delinsTG	XP_024308855.1:n.2007-50_2007-49delinsTG
XM_024453088.1:c.2007-50_2007-49delinsTG	XP_024308856.1:n.2007-50_2007-49delinsTG
XM_024453089.1:c.2007-50_2007-49delinsTG	XP_024308857.1:n.2007-50_2007-49delinsTG
XM_024453090.1:c.2043-50_2043-49delinsTG	XP_024308858.1:n.2043-50_2043-49delinsTG
XM_024453091.1:c.1872-50_1872-49delinsTG	XP_024308859.1:n.1872-50_1872-49delinsTG
XM_024453092.1:c.1872-50_1872-49delinsTG	XP_024308860.1:n.1872-50_1872-49delinsTG
XM_024453093.1:c.1524-50_1524-49delinsTG	XP_024308861.1:n.1524-50_1524-49delinsTG
NM_001206744.2:c.2007-50_2007-49delinsTG MANE Select	NP_001193673.1:n.2007-50_2007-49delinsTG
NM_000547.6:c.2007-50_2007-49delinsTG	NP_000538.3:n.2007-50_2007-49delinsTG
NM_001206745.2:c.1836-50_1836-49delinsTG	NP_001193674.1:n.1836-50_1836-49delinsTG
NM_175719.4:c.1836-50_1836-49delinsTG	NP_783650.1:n.1836-50_1836-49delinsTG