Canonical Allele Identifier: CA758563869

Gene: TPO

Linked Data

• dbSNP Id: rs72230434
• gnomAD v3: 2-1487738-C-CAAA
• gnomAD v4: 2-1487738-C-CAAA
• MyVariant Identifiers: chr2:g.1491510_1491511insAAA (hg19) ; chr2:g.1487738_1487739insAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487750_1487752dup , CM000664.2:g.1487750_1487752dup	GRCh38
NC_000002.11:g.1491522_1491524dup , CM000664.1:g.1491522_1491524dup	GRCh37
NC_000002.10:g.1470529_1470531dup	NCBI36
NG_011581.1:g.79288_79290dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1598-71_1598-69dup MANE Select	ENSP00000329869.4:n.1598-71_1598-69dup
ENST00000329066.8:c.1598-71_1598-69dup	ENSP00000329869.4:n.1598-71_1598-69dup
ENST00000345913.8:c.1598-71_1598-69dup	ENSP00000318820.7:n.1598-71_1598-69dup
ENST00000346956.7:c.1598-71_1598-69dup	ENSP00000263886.6:n.1598-71_1598-69dup
ENST00000382198.5:c.1079-71_1079-69dup	ENSP00000371633.1:n.1079-71_1079-69dup
ENST00000382201.7:c.1597+2896_1597+2898dup	ENSP00000371636.3:n.1597+2896_1597+2898dup
ENST00000422464.5:c.1385-71_1385-69dup	ENSP00000405788.1:n.1385-71_1385-69dup
ENST00000446278.5:c.192+2896_192+2898dup
ENST00000462973.5:n.186+2896_186+2898dup
ENST00000469607.3:c.190+2896_190+2898dup	ENSP00000419461.1:n.190+2896_190+2898dup
ENST00000497517.6:n.439+2896_439+2898dup
NM_000547.5:c.1598-71_1598-69dup	NP_000538.3:n.1598-71_1598-69dup
NM_001206744.1:c.1598-71_1598-69dup	NP_001193673.1:n.1598-71_1598-69dup
NM_001206745.1:c.1597+2896_1597+2898dup	NP_001193674.1:n.1597+2896_1597+2898dup
NM_175719.3:c.1597+2896_1597+2898dup	NP_783650.1:n.1597+2896_1597+2898dup
NM_175721.3:c.1598-71_1598-69dup	NP_783652.1:n.1598-71_1598-69dup
NM_175722.3:c.1079-71_1079-69dup	NP_783653.1:n.1079-71_1079-69dup
XM_011510379.1:c.1598-71_1598-69dup	XP_011508681.1:n.1598-71_1598-69dup
XM_011510380.1:c.1598-71_1598-69dup	XP_011508682.1:n.1598-71_1598-69dup
XM_011510381.1:c.1597+2896_1597+2898dup	XP_011508683.1:n.1597+2896_1597+2898dup
XR_922681.1:n.1599-71_1599-69dup
XM_011510380.3:c.1634-71_1634-69dup	XP_011508682.2:n.1634-71_1634-69dup
XM_024453085.1:c.1634-71_1634-69dup	XP_024308853.1:n.1634-71_1634-69dup
XM_024453086.1:c.1634-71_1634-69dup	XP_024308854.1:n.1634-71_1634-69dup
XM_024453087.1:c.1598-71_1598-69dup	XP_024308855.1:n.1598-71_1598-69dup
XM_024453088.1:c.1598-71_1598-69dup	XP_024308856.1:n.1598-71_1598-69dup
XM_024453089.1:c.1598-71_1598-69dup	XP_024308857.1:n.1598-71_1598-69dup
XM_024453090.1:c.1634-71_1634-69dup	XP_024308858.1:n.1634-71_1634-69dup
XM_024453091.1:c.1633+2896_1633+2898dup	XP_024308859.1:n.1633+2896_1633+2898dup
XM_024453092.1:c.1633+2896_1633+2898dup	XP_024308860.1:n.1633+2896_1633+2898dup
XM_024453093.1:c.1115-71_1115-69dup	XP_024308861.1:n.1115-71_1115-69dup
NM_001206744.2:c.1598-71_1598-69dup MANE Select	NP_001193673.1:n.1598-71_1598-69dup
NM_000547.6:c.1598-71_1598-69dup	NP_000538.3:n.1598-71_1598-69dup
NM_001206745.2:c.1597+2896_1597+2898dup	NP_001193674.1:n.1597+2896_1597+2898dup
NM_175719.4:c.1597+2896_1597+2898dup	NP_783650.1:n.1597+2896_1597+2898dup