Canonical Allele Identifier: CA2657646467

Gene: TPO

Linked Data

• gnomAD v4: 2-1487743-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487743_1487744insG , CM000664.2:g.1487743_1487744insG	GRCh38
NC_000002.11:g.1491515_1491516insG , CM000664.1:g.1491515_1491516insG	GRCh37
NC_000002.10:g.1470522_1470523insG	NCBI36
NG_011581.1:g.79281_79282insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1598-78_1598-77insG MANE Select	ENSP00000329869.4:n.1598-78_1598-77insG
ENST00000329066.8:c.1598-78_1598-77insG	ENSP00000329869.4:n.1598-78_1598-77insG
ENST00000345913.8:c.1598-78_1598-77insG	ENSP00000318820.7:n.1598-78_1598-77insG
ENST00000346956.7:c.1598-78_1598-77insG	ENSP00000263886.6:n.1598-78_1598-77insG
ENST00000382198.5:c.1079-78_1079-77insG	ENSP00000371633.1:n.1079-78_1079-77insG
ENST00000382201.7:c.1597+2889_1597+2890insG	ENSP00000371636.3:n.1597+2889_1597+2890insG
ENST00000422464.5:c.1385-78_1385-77insG	ENSP00000405788.1:n.1385-78_1385-77insG
ENST00000446278.5:c.192+2889_192+2890insG
ENST00000462973.5:n.186+2889_186+2890insG
ENST00000469607.3:c.190+2889_190+2890insG	ENSP00000419461.1:n.190+2889_190+2890insG
ENST00000497517.6:n.439+2889_439+2890insG
NM_000547.5:c.1598-78_1598-77insG	NP_000538.3:n.1598-78_1598-77insG
NM_001206744.1:c.1598-78_1598-77insG	NP_001193673.1:n.1598-78_1598-77insG
NM_001206745.1:c.1597+2889_1597+2890insG	NP_001193674.1:n.1597+2889_1597+2890insG
NM_175719.3:c.1597+2889_1597+2890insG	NP_783650.1:n.1597+2889_1597+2890insG
NM_175721.3:c.1598-78_1598-77insG	NP_783652.1:n.1598-78_1598-77insG
NM_175722.3:c.1079-78_1079-77insG	NP_783653.1:n.1079-78_1079-77insG
XM_011510379.1:c.1598-78_1598-77insG	XP_011508681.1:n.1598-78_1598-77insG
XM_011510380.1:c.1598-78_1598-77insG	XP_011508682.1:n.1598-78_1598-77insG
XM_011510381.1:c.1597+2889_1597+2890insG	XP_011508683.1:n.1597+2889_1597+2890insG
XR_922681.1:n.1599-78_1599-77insG
XM_011510380.3:c.1634-78_1634-77insG	XP_011508682.2:n.1634-78_1634-77insG
XM_024453085.1:c.1634-78_1634-77insG	XP_024308853.1:n.1634-78_1634-77insG
XM_024453086.1:c.1634-78_1634-77insG	XP_024308854.1:n.1634-78_1634-77insG
XM_024453087.1:c.1598-78_1598-77insG	XP_024308855.1:n.1598-78_1598-77insG
XM_024453088.1:c.1598-78_1598-77insG	XP_024308856.1:n.1598-78_1598-77insG
XM_024453089.1:c.1598-78_1598-77insG	XP_024308857.1:n.1598-78_1598-77insG
XM_024453090.1:c.1634-78_1634-77insG	XP_024308858.1:n.1634-78_1634-77insG
XM_024453091.1:c.1633+2889_1633+2890insG	XP_024308859.1:n.1633+2889_1633+2890insG
XM_024453092.1:c.1633+2889_1633+2890insG	XP_024308860.1:n.1633+2889_1633+2890insG
XM_024453093.1:c.1115-78_1115-77insG	XP_024308861.1:n.1115-78_1115-77insG
NM_001206744.2:c.1598-78_1598-77insG MANE Select	NP_001193673.1:n.1598-78_1598-77insG
NM_000547.6:c.1598-78_1598-77insG	NP_000538.3:n.1598-78_1598-77insG
NM_001206745.2:c.1597+2889_1597+2890insG	NP_001193674.1:n.1597+2889_1597+2890insG
NM_175719.4:c.1597+2889_1597+2890insG	NP_783650.1:n.1597+2889_1597+2890insG