Canonical Allele Identifier: CA41417065

Gene: TPO

Linked Data

• dbSNP Id: rs1000651665
• gnomAD v3: 2-1487701-C-CTCCA
• gnomAD v4: 2-1487701-C-CTCCA
• MyVariant Identifiers: chr2:g.1491473_1491474insTCCA (hg19) ; chr2:g.1487701_1487702insTCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487702_1487705dup , CM000664.2:g.1487702_1487705dup	GRCh38
NC_000002.11:g.1491474_1491477dup , CM000664.1:g.1491474_1491477dup	GRCh37
NC_000002.10:g.1470481_1470484dup	NCBI36
NG_011581.1:g.79240_79243dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1598-119_1598-116dup MANE Select	ENSP00000329869.4:n.1598-119_1598-116dup
ENST00000329066.8:c.1598-119_1598-116dup	ENSP00000329869.4:n.1598-119_1598-116dup
ENST00000345913.8:c.1598-119_1598-116dup	ENSP00000318820.7:n.1598-119_1598-116dup
ENST00000346956.7:c.1598-119_1598-116dup	ENSP00000263886.6:n.1598-119_1598-116dup
ENST00000382198.5:c.1079-119_1079-116dup	ENSP00000371633.1:n.1079-119_1079-116dup
ENST00000382201.7:c.1597+2848_1597+2851dup	ENSP00000371636.3:n.1597+2848_1597+2851dup
ENST00000422464.5:c.1385-119_1385-116dup	ENSP00000405788.1:n.1385-119_1385-116dup
ENST00000446278.5:c.192+2848_192+2851dup
ENST00000462973.5:n.186+2848_186+2851dup
ENST00000469607.3:c.190+2848_190+2851dup	ENSP00000419461.1:n.190+2848_190+2851dup
ENST00000497517.6:n.439+2848_439+2851dup
NM_000547.5:c.1598-119_1598-116dup	NP_000538.3:n.1598-119_1598-116dup
NM_001206744.1:c.1598-119_1598-116dup	NP_001193673.1:n.1598-119_1598-116dup
NM_001206745.1:c.1597+2848_1597+2851dup	NP_001193674.1:n.1597+2848_1597+2851dup
NM_175719.3:c.1597+2848_1597+2851dup	NP_783650.1:n.1597+2848_1597+2851dup
NM_175721.3:c.1598-119_1598-116dup	NP_783652.1:n.1598-119_1598-116dup
NM_175722.3:c.1079-119_1079-116dup	NP_783653.1:n.1079-119_1079-116dup
XM_011510379.1:c.1598-119_1598-116dup	XP_011508681.1:n.1598-119_1598-116dup
XM_011510380.1:c.1598-119_1598-116dup	XP_011508682.1:n.1598-119_1598-116dup
XM_011510381.1:c.1597+2848_1597+2851dup	XP_011508683.1:n.1597+2848_1597+2851dup
XR_922681.1:n.1599-119_1599-116dup
XM_011510380.3:c.1634-119_1634-116dup	XP_011508682.2:n.1634-119_1634-116dup
XM_024453085.1:c.1634-119_1634-116dup	XP_024308853.1:n.1634-119_1634-116dup
XM_024453086.1:c.1634-119_1634-116dup	XP_024308854.1:n.1634-119_1634-116dup
XM_024453087.1:c.1598-119_1598-116dup	XP_024308855.1:n.1598-119_1598-116dup
XM_024453088.1:c.1598-119_1598-116dup	XP_024308856.1:n.1598-119_1598-116dup
XM_024453089.1:c.1598-119_1598-116dup	XP_024308857.1:n.1598-119_1598-116dup
XM_024453090.1:c.1634-119_1634-116dup	XP_024308858.1:n.1634-119_1634-116dup
XM_024453091.1:c.1633+2848_1633+2851dup	XP_024308859.1:n.1633+2848_1633+2851dup
XM_024453092.1:c.1633+2848_1633+2851dup	XP_024308860.1:n.1633+2848_1633+2851dup
XM_024453093.1:c.1115-119_1115-116dup	XP_024308861.1:n.1115-119_1115-116dup
NM_001206744.2:c.1598-119_1598-116dup MANE Select	NP_001193673.1:n.1598-119_1598-116dup
NM_000547.6:c.1598-119_1598-116dup	NP_000538.3:n.1598-119_1598-116dup
NM_001206745.2:c.1597+2848_1597+2851dup	NP_001193674.1:n.1597+2848_1597+2851dup
NM_175719.4:c.1597+2848_1597+2851dup	NP_783650.1:n.1597+2848_1597+2851dup