Canonical Allele Identifier: CA1233573496

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487754_1487756delinsTGA , CM000664.2:g.1487754_1487756delinsTGA	GRCh38
NC_000002.11:g.1491526_1491528delinsTGA , CM000664.1:g.1491526_1491528delinsTGA	GRCh37
NC_000002.10:g.1470533_1470535delinsTGA	NCBI36
NG_011581.1:g.79292_79294delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1598-67_1598-65delinsTGA MANE Select	ENSP00000329869.4:n.1598-67_1598-65delinsTGA
ENST00000329066.8:c.1598-67_1598-65delinsTGA	ENSP00000329869.4:n.1598-67_1598-65delinsTGA
ENST00000345913.8:c.1598-67_1598-65delinsTGA	ENSP00000318820.7:n.1598-67_1598-65delinsTGA
ENST00000346956.7:c.1598-67_1598-65delinsTGA	ENSP00000263886.6:n.1598-67_1598-65delinsTGA
ENST00000382198.5:c.1079-67_1079-65delinsTGA	ENSP00000371633.1:n.1079-67_1079-65delinsTGA
ENST00000382201.7:c.1597+2900_1597+2902delinsTGA	ENSP00000371636.3:n.1597+2900_1597+2902delinsTGA
ENST00000422464.5:c.1385-67_1385-65delinsTGA	ENSP00000405788.1:n.1385-67_1385-65delinsTGA
ENST00000446278.5:c.192+2900_192+2902delinsTGA
ENST00000462973.5:n.186+2900_186+2902delinsTGA
ENST00000469607.3:c.190+2900_190+2902delinsTGA	ENSP00000419461.1:n.190+2900_190+2902delinsTGA
ENST00000497517.6:n.439+2900_439+2902delinsTGA
NM_000547.5:c.1598-67_1598-65delinsTGA	NP_000538.3:n.1598-67_1598-65delinsTGA
NM_001206744.1:c.1598-67_1598-65delinsTGA	NP_001193673.1:n.1598-67_1598-65delinsTGA
NM_001206745.1:c.1597+2900_1597+2902delinsTGA	NP_001193674.1:n.1597+2900_1597+2902delinsTGA
NM_175719.3:c.1597+2900_1597+2902delinsTGA	NP_783650.1:n.1597+2900_1597+2902delinsTGA
NM_175721.3:c.1598-67_1598-65delinsTGA	NP_783652.1:n.1598-67_1598-65delinsTGA
NM_175722.3:c.1079-67_1079-65delinsTGA	NP_783653.1:n.1079-67_1079-65delinsTGA
XM_011510379.1:c.1598-67_1598-65delinsTGA	XP_011508681.1:n.1598-67_1598-65delinsTGA
XM_011510380.1:c.1598-67_1598-65delinsTGA	XP_011508682.1:n.1598-67_1598-65delinsTGA
XM_011510381.1:c.1597+2900_1597+2902delinsTGA	XP_011508683.1:n.1597+2900_1597+2902delinsTGA
XR_922681.1:n.1599-67_1599-65delinsTGA
XM_011510380.3:c.1634-67_1634-65delinsTGA	XP_011508682.2:n.1634-67_1634-65delinsTGA
XM_024453085.1:c.1634-67_1634-65delinsTGA	XP_024308853.1:n.1634-67_1634-65delinsTGA
XM_024453086.1:c.1634-67_1634-65delinsTGA	XP_024308854.1:n.1634-67_1634-65delinsTGA
XM_024453087.1:c.1598-67_1598-65delinsTGA	XP_024308855.1:n.1598-67_1598-65delinsTGA
XM_024453088.1:c.1598-67_1598-65delinsTGA	XP_024308856.1:n.1598-67_1598-65delinsTGA
XM_024453089.1:c.1598-67_1598-65delinsTGA	XP_024308857.1:n.1598-67_1598-65delinsTGA
XM_024453090.1:c.1634-67_1634-65delinsTGA	XP_024308858.1:n.1634-67_1634-65delinsTGA
XM_024453091.1:c.1633+2900_1633+2902delinsTGA	XP_024308859.1:n.1633+2900_1633+2902delinsTGA
XM_024453092.1:c.1633+2900_1633+2902delinsTGA	XP_024308860.1:n.1633+2900_1633+2902delinsTGA
XM_024453093.1:c.1115-67_1115-65delinsTGA	XP_024308861.1:n.1115-67_1115-65delinsTGA
NM_001206744.2:c.1598-67_1598-65delinsTGA MANE Select	NP_001193673.1:n.1598-67_1598-65delinsTGA
NM_000547.6:c.1598-67_1598-65delinsTGA	NP_000538.3:n.1598-67_1598-65delinsTGA
NM_001206745.2:c.1597+2900_1597+2902delinsTGA	NP_001193674.1:n.1597+2900_1597+2902delinsTGA
NM_175719.4:c.1597+2900_1597+2902delinsTGA	NP_783650.1:n.1597+2900_1597+2902delinsTGA