Canonical Allele Identifier: CA2657646499

Gene: TPO

Linked Data

• gnomAD v4: 2-1487992-G-GTCTGCCAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487995_1488003dup , CM000664.2:g.1487995_1488003dup	GRCh38
NC_000002.11:g.1491767_1491775dup , CM000664.1:g.1491767_1491775dup	GRCh37
NC_000002.10:g.1470774_1470782dup	NCBI36
NG_011581.1:g.79533_79541dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1768+4_1768+12dup MANE Select	ENSP00000329869.4:n.1768+4_1768+12dup
ENST00000329066.8:c.1768+4_1768+12dup	ENSP00000329869.4:n.1768+4_1768+12dup
ENST00000345913.8:c.1768+4_1768+12dup	ENSP00000318820.7:n.1768+4_1768+12dup
ENST00000346956.7:c.1768+4_1768+12dup	ENSP00000263886.6:n.1768+4_1768+12dup
ENST00000382198.5:c.1249+4_1249+12dup	ENSP00000371633.1:n.1249+4_1249+12dup
ENST00000382201.7:c.1597+3141_1597+3149dup	ENSP00000371636.3:n.1597+3141_1597+3149dup
ENST00000422464.5:c.1555+4_1555+12dup	ENSP00000405788.1:n.1555+4_1555+12dup
ENST00000446278.5:c.192+3141_192+3149dup
ENST00000462973.5:n.186+3141_186+3149dup
ENST00000469607.3:c.190+3141_190+3149dup	ENSP00000419461.1:n.190+3141_190+3149dup
ENST00000497517.6:n.439+3141_439+3149dup
NM_000547.5:c.1768+4_1768+12dup	NP_000538.3:n.1768+4_1768+12dup
NM_001206744.1:c.1768+4_1768+12dup	NP_001193673.1:n.1768+4_1768+12dup
NM_001206745.1:c.1597+3141_1597+3149dup	NP_001193674.1:n.1597+3141_1597+3149dup
NM_175719.3:c.1597+3141_1597+3149dup	NP_783650.1:n.1597+3141_1597+3149dup
NM_175721.3:c.1768+4_1768+12dup	NP_783652.1:n.1768+4_1768+12dup
NM_175722.3:c.1249+4_1249+12dup	NP_783653.1:n.1249+4_1249+12dup
XM_011510379.1:c.1768+4_1768+12dup	XP_011508681.1:n.1768+4_1768+12dup
XM_011510380.1:c.1768+4_1768+12dup	XP_011508682.1:n.1768+4_1768+12dup
XM_011510381.1:c.1597+3141_1597+3149dup	XP_011508683.1:n.1597+3141_1597+3149dup
XR_922681.1:n.1769+4_1769+12dup
XM_011510380.3:c.1804+4_1804+12dup	XP_011508682.2:n.1804+4_1804+12dup
XM_024453085.1:c.1804+4_1804+12dup	XP_024308853.1:n.1804+4_1804+12dup
XM_024453086.1:c.1804+4_1804+12dup	XP_024308854.1:n.1804+4_1804+12dup
XM_024453087.1:c.1768+4_1768+12dup	XP_024308855.1:n.1768+4_1768+12dup
XM_024453088.1:c.1768+4_1768+12dup	XP_024308856.1:n.1768+4_1768+12dup
XM_024453089.1:c.1768+4_1768+12dup	XP_024308857.1:n.1768+4_1768+12dup
XM_024453090.1:c.1804+4_1804+12dup	XP_024308858.1:n.1804+4_1804+12dup
XM_024453091.1:c.1633+3141_1633+3149dup	XP_024308859.1:n.1633+3141_1633+3149dup
XM_024453092.1:c.1633+3141_1633+3149dup	XP_024308860.1:n.1633+3141_1633+3149dup
XM_024453093.1:c.1285+4_1285+12dup	XP_024308861.1:n.1285+4_1285+12dup
NM_001206744.2:c.1768+4_1768+12dup MANE Select	NP_001193673.1:n.1768+4_1768+12dup
NM_000547.6:c.1768+4_1768+12dup	NP_000538.3:n.1768+4_1768+12dup
NM_001206745.2:c.1597+3141_1597+3149dup	NP_001193674.1:n.1597+3141_1597+3149dup
NM_175719.4:c.1597+3141_1597+3149dup	NP_783650.1:n.1597+3141_1597+3149dup