Canonical Allele Identifier: CA2586968654

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487944_1487949del , CM000664.2:g.1487944_1487949del	GRCh38
NC_000002.11:g.1491716_1491721del , CM000664.1:g.1491716_1491721del	GRCh37
NC_000002.10:g.1470723_1470728del	NCBI36
NG_011581.1:g.79482_79487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1721_1726del MANE Select	ENSP00000329869.4:p.Asp574_Leu575del
ENST00000329066.8:c.1721_1726del	ENSP00000329869.4:p.Asp574_Leu575del
ENST00000345913.8:c.1721_1726del	ENSP00000318820.7:p.Asp574_Leu575del
ENST00000346956.7:c.1721_1726del	ENSP00000263886.6:p.Asp574_Leu575del
ENST00000382198.5:c.1202_1207del	ENSP00000371633.1:p.Asp401_Leu402del
ENST00000382201.7:c.1597+3090_1597+3095del	ENSP00000371636.3:n.1597+3090_1597+3095del
ENST00000422464.5:c.1508_1513del	ENSP00000405788.1:p.Asp503_Leu504del
ENST00000446278.5:c.192+3090_192+3095del
ENST00000462973.5:n.186+3090_186+3095del
ENST00000469607.3:c.190+3090_190+3095del	ENSP00000419461.1:n.190+3090_190+3095del
ENST00000497517.6:n.439+3090_439+3095del
NM_000547.5:c.1721_1726del	NP_000538.3:p.Asp574_Leu575del
NM_001206744.1:c.1721_1726del	NP_001193673.1:p.Asp574_Leu575del
NM_001206745.1:c.1597+3090_1597+3095del	NP_001193674.1:n.1597+3090_1597+3095del
NM_175719.3:c.1597+3090_1597+3095del	NP_783650.1:n.1597+3090_1597+3095del
NM_175721.3:c.1721_1726del	NP_783652.1:p.Asp574_Leu575del
NM_175722.3:c.1202_1207del	NP_783653.1:p.Asp401_Leu402del
XM_011510379.1:c.1721_1726del	XP_011508681.1:p.Asp574_Leu575del
XM_011510380.1:c.1721_1726del	XP_011508682.1:p.Asp574_Leu575del
XM_011510381.1:c.1597+3090_1597+3095del	XP_011508683.1:n.1597+3090_1597+3095del
XR_922681.1:n.1722_1727del
XM_011510380.3:c.1757_1762del	XP_011508682.2:p.Asp586_Leu587del
XM_024453085.1:c.1757_1762del	XP_024308853.1:p.Asp586_Leu587del
XM_024453086.1:c.1757_1762del	XP_024308854.1:p.Asp586_Leu587del
XM_024453087.1:c.1721_1726del	XP_024308855.1:p.Asp574_Leu575del
XM_024453088.1:c.1721_1726del	XP_024308856.1:p.Asp574_Leu575del
XM_024453089.1:c.1721_1726del	XP_024308857.1:p.Asp574_Leu575del
XM_024453090.1:c.1757_1762del	XP_024308858.1:p.Asp586_Leu587del
XM_024453091.1:c.1633+3090_1633+3095del	XP_024308859.1:n.1633+3090_1633+3095del
XM_024453092.1:c.1633+3090_1633+3095del	XP_024308860.1:n.1633+3090_1633+3095del
XM_024453093.1:c.1238_1243del	XP_024308861.1:p.Asp413_Leu414del
NM_001206744.2:c.1721_1726del MANE Select	NP_001193673.1:p.Asp574_Leu575del
NM_000547.6:c.1721_1726del	NP_000538.3:p.Asp574_Leu575del
NM_001206745.2:c.1597+3090_1597+3095del	NP_001193674.1:n.1597+3090_1597+3095del
NM_175719.4:c.1597+3090_1597+3095del	NP_783650.1:n.1597+3090_1597+3095del