Canonical Allele Identifier: CA2657646471

Gene: TPO

Linked Data

• gnomAD v4: 2-1487751-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487752_1487753del , CM000664.2:g.1487752_1487753del	GRCh38
NC_000002.11:g.1491524_1491525del , CM000664.1:g.1491524_1491525del	GRCh37
NC_000002.10:g.1470531_1470532del	NCBI36
NG_011581.1:g.79290_79291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1598-69_1598-68del MANE Select	ENSP00000329869.4:n.1598-69_1598-68del
ENST00000329066.8:c.1598-69_1598-68del	ENSP00000329869.4:n.1598-69_1598-68del
ENST00000345913.8:c.1598-69_1598-68del	ENSP00000318820.7:n.1598-69_1598-68del
ENST00000346956.7:c.1598-69_1598-68del	ENSP00000263886.6:n.1598-69_1598-68del
ENST00000382198.5:c.1079-69_1079-68del	ENSP00000371633.1:n.1079-69_1079-68del
ENST00000382201.7:c.1597+2898_1597+2899del	ENSP00000371636.3:n.1597+2898_1597+2899del
ENST00000422464.5:c.1385-69_1385-68del	ENSP00000405788.1:n.1385-69_1385-68del
ENST00000446278.5:c.192+2898_192+2899del
ENST00000462973.5:n.186+2898_186+2899del
ENST00000469607.3:c.190+2898_190+2899del	ENSP00000419461.1:n.190+2898_190+2899del
ENST00000497517.6:n.439+2898_439+2899del
NM_000547.5:c.1598-69_1598-68del	NP_000538.3:n.1598-69_1598-68del
NM_001206744.1:c.1598-69_1598-68del	NP_001193673.1:n.1598-69_1598-68del
NM_001206745.1:c.1597+2898_1597+2899del	NP_001193674.1:n.1597+2898_1597+2899del
NM_175719.3:c.1597+2898_1597+2899del	NP_783650.1:n.1597+2898_1597+2899del
NM_175721.3:c.1598-69_1598-68del	NP_783652.1:n.1598-69_1598-68del
NM_175722.3:c.1079-69_1079-68del	NP_783653.1:n.1079-69_1079-68del
XM_011510379.1:c.1598-69_1598-68del	XP_011508681.1:n.1598-69_1598-68del
XM_011510380.1:c.1598-69_1598-68del	XP_011508682.1:n.1598-69_1598-68del
XM_011510381.1:c.1597+2898_1597+2899del	XP_011508683.1:n.1597+2898_1597+2899del
XR_922681.1:n.1599-69_1599-68del
XM_011510380.3:c.1634-69_1634-68del	XP_011508682.2:n.1634-69_1634-68del
XM_024453085.1:c.1634-69_1634-68del	XP_024308853.1:n.1634-69_1634-68del
XM_024453086.1:c.1634-69_1634-68del	XP_024308854.1:n.1634-69_1634-68del
XM_024453087.1:c.1598-69_1598-68del	XP_024308855.1:n.1598-69_1598-68del
XM_024453088.1:c.1598-69_1598-68del	XP_024308856.1:n.1598-69_1598-68del
XM_024453089.1:c.1598-69_1598-68del	XP_024308857.1:n.1598-69_1598-68del
XM_024453090.1:c.1634-69_1634-68del	XP_024308858.1:n.1634-69_1634-68del
XM_024453091.1:c.1633+2898_1633+2899del	XP_024308859.1:n.1633+2898_1633+2899del
XM_024453092.1:c.1633+2898_1633+2899del	XP_024308860.1:n.1633+2898_1633+2899del
XM_024453093.1:c.1115-69_1115-68del	XP_024308861.1:n.1115-69_1115-68del
NM_001206744.2:c.1598-69_1598-68del MANE Select	NP_001193673.1:n.1598-69_1598-68del
NM_000547.6:c.1598-69_1598-68del	NP_000538.3:n.1598-69_1598-68del
NM_001206745.2:c.1597+2898_1597+2899del	NP_001193674.1:n.1597+2898_1597+2899del
NM_175719.4:c.1597+2898_1597+2899del	NP_783650.1:n.1597+2898_1597+2899del