Canonical Allele Identifier: CA1233577762

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1495854_1495855delinsGC , CM000664.2:g.1495854_1495855delinsGC	GRCh38
NC_000002.11:g.1499626_1499627delinsGC , CM000664.1:g.1499626_1499627delinsGC	GRCh37
NC_000002.10:g.1478633_1478634delinsGC	NCBI36
NG_011581.1:g.87392_87393delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2007-135_2007-134delinsGC MANE Select	ENSP00000329869.4:n.2007-135_2007-134delinsGC
ENST00000329066.8:c.2007-135_2007-134delinsGC	ENSP00000329869.4:n.2007-135_2007-134delinsGC
ENST00000345913.8:c.2007-135_2007-134delinsGC	ENSP00000318820.7:n.2007-135_2007-134delinsGC
ENST00000346956.7:c.2007-135_2007-134delinsGC	ENSP00000263886.6:n.2007-135_2007-134delinsGC
ENST00000382198.5:c.1488-135_1488-134delinsGC	ENSP00000371633.1:n.1488-135_1488-134delinsGC
ENST00000382201.7:c.1836-135_1836-134delinsGC	ENSP00000371636.3:n.1836-135_1836-134delinsGC
ENST00000422464.5:c.1794-135_1794-134delinsGC	ENSP00000405788.1:n.1794-135_1794-134delinsGC
ENST00000446278.5:c.431-135_431-134delinsGC
ENST00000462973.5:n.424+1815_424+1816delinsGC
ENST00000469607.3:c.429-135_429-134delinsGC	ENSP00000419461.1:n.429-135_429-134delinsGC
ENST00000497517.6:n.677+1815_677+1816delinsGC
NM_000547.5:c.2007-135_2007-134delinsGC	NP_000538.3:n.2007-135_2007-134delinsGC
NM_001206744.1:c.2007-135_2007-134delinsGC	NP_001193673.1:n.2007-135_2007-134delinsGC
NM_001206745.1:c.1836-135_1836-134delinsGC	NP_001193674.1:n.1836-135_1836-134delinsGC
NM_175719.3:c.1836-135_1836-134delinsGC	NP_783650.1:n.1836-135_1836-134delinsGC
NM_175721.3:c.2007-135_2007-134delinsGC	NP_783652.1:n.2007-135_2007-134delinsGC
NM_175722.3:c.1488-135_1488-134delinsGC	NP_783653.1:n.1488-135_1488-134delinsGC
XM_011510379.1:c.2007-135_2007-134delinsGC	XP_011508681.1:n.2007-135_2007-134delinsGC
XM_011510380.1:c.2007-135_2007-134delinsGC	XP_011508682.1:n.2007-135_2007-134delinsGC
XM_011510381.1:c.1836-135_1836-134delinsGC	XP_011508683.1:n.1836-135_1836-134delinsGC
XR_922681.1:n.2008-135_2008-134delinsGC
XM_011510380.3:c.2043-135_2043-134delinsGC	XP_011508682.2:n.2043-135_2043-134delinsGC
XM_024453085.1:c.2043-135_2043-134delinsGC	XP_024308853.1:n.2043-135_2043-134delinsGC
XM_024453086.1:c.2043-135_2043-134delinsGC	XP_024308854.1:n.2043-135_2043-134delinsGC
XM_024453087.1:c.2007-135_2007-134delinsGC	XP_024308855.1:n.2007-135_2007-134delinsGC
XM_024453088.1:c.2007-135_2007-134delinsGC	XP_024308856.1:n.2007-135_2007-134delinsGC
XM_024453089.1:c.2007-135_2007-134delinsGC	XP_024308857.1:n.2007-135_2007-134delinsGC
XM_024453090.1:c.2043-135_2043-134delinsGC	XP_024308858.1:n.2043-135_2043-134delinsGC
XM_024453091.1:c.1872-135_1872-134delinsGC	XP_024308859.1:n.1872-135_1872-134delinsGC
XM_024453092.1:c.1872-135_1872-134delinsGC	XP_024308860.1:n.1872-135_1872-134delinsGC
XM_024453093.1:c.1524-135_1524-134delinsGC	XP_024308861.1:n.1524-135_1524-134delinsGC
NM_001206744.2:c.2007-135_2007-134delinsGC MANE Select	NP_001193673.1:n.2007-135_2007-134delinsGC
NM_000547.6:c.2007-135_2007-134delinsGC	NP_000538.3:n.2007-135_2007-134delinsGC
NM_001206745.2:c.1836-135_1836-134delinsGC	NP_001193674.1:n.1836-135_1836-134delinsGC
NM_175719.4:c.1836-135_1836-134delinsGC	NP_783650.1:n.1836-135_1836-134delinsGC