Canonical Allele Identifier: CA1026814970

Gene: TPO

Linked Data

• gnomAD v3: 2-1487734-GTCTC-G
• gnomAD v4: 2-1487734-GTCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1487735_1487738del , CM000664.2:g.1487735_1487738del	GRCh38
NC_000002.11:g.1491507_1491510del , CM000664.1:g.1491507_1491510del	GRCh37
NC_000002.10:g.1470514_1470517del	NCBI36
NG_011581.1:g.79273_79276del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1598-86_1598-83del MANE Select	ENSP00000329869.4:n.1598-86_1598-83del
ENST00000329066.8:c.1598-86_1598-83del	ENSP00000329869.4:n.1598-86_1598-83del
ENST00000345913.8:c.1598-86_1598-83del	ENSP00000318820.7:n.1598-86_1598-83del
ENST00000346956.7:c.1598-86_1598-83del	ENSP00000263886.6:n.1598-86_1598-83del
ENST00000382198.5:c.1079-86_1079-83del	ENSP00000371633.1:n.1079-86_1079-83del
ENST00000382201.7:c.1597+2881_1597+2884del	ENSP00000371636.3:n.1597+2881_1597+2884del
ENST00000422464.5:c.1385-86_1385-83del	ENSP00000405788.1:n.1385-86_1385-83del
ENST00000446278.5:c.192+2881_192+2884del
ENST00000462973.5:n.186+2881_186+2884del
ENST00000469607.3:c.190+2881_190+2884del	ENSP00000419461.1:n.190+2881_190+2884del
ENST00000497517.6:n.439+2881_439+2884del
NM_000547.5:c.1598-86_1598-83del	NP_000538.3:n.1598-86_1598-83del
NM_001206744.1:c.1598-86_1598-83del	NP_001193673.1:n.1598-86_1598-83del
NM_001206745.1:c.1597+2881_1597+2884del	NP_001193674.1:n.1597+2881_1597+2884del
NM_175719.3:c.1597+2881_1597+2884del	NP_783650.1:n.1597+2881_1597+2884del
NM_175721.3:c.1598-86_1598-83del	NP_783652.1:n.1598-86_1598-83del
NM_175722.3:c.1079-86_1079-83del	NP_783653.1:n.1079-86_1079-83del
XM_011510379.1:c.1598-86_1598-83del	XP_011508681.1:n.1598-86_1598-83del
XM_011510380.1:c.1598-86_1598-83del	XP_011508682.1:n.1598-86_1598-83del
XM_011510381.1:c.1597+2881_1597+2884del	XP_011508683.1:n.1597+2881_1597+2884del
XR_922681.1:n.1599-86_1599-83del
XM_011510380.3:c.1634-86_1634-83del	XP_011508682.2:n.1634-86_1634-83del
XM_024453085.1:c.1634-86_1634-83del	XP_024308853.1:n.1634-86_1634-83del
XM_024453086.1:c.1634-86_1634-83del	XP_024308854.1:n.1634-86_1634-83del
XM_024453087.1:c.1598-86_1598-83del	XP_024308855.1:n.1598-86_1598-83del
XM_024453088.1:c.1598-86_1598-83del	XP_024308856.1:n.1598-86_1598-83del
XM_024453089.1:c.1598-86_1598-83del	XP_024308857.1:n.1598-86_1598-83del
XM_024453090.1:c.1634-86_1634-83del	XP_024308858.1:n.1634-86_1634-83del
XM_024453091.1:c.1633+2881_1633+2884del	XP_024308859.1:n.1633+2881_1633+2884del
XM_024453092.1:c.1633+2881_1633+2884del	XP_024308860.1:n.1633+2881_1633+2884del
XM_024453093.1:c.1115-86_1115-83del	XP_024308861.1:n.1115-86_1115-83del
NM_001206744.2:c.1598-86_1598-83del MANE Select	NP_001193673.1:n.1598-86_1598-83del
NM_000547.6:c.1598-86_1598-83del	NP_000538.3:n.1598-86_1598-83del
NM_001206745.2:c.1597+2881_1597+2884del	NP_001193674.1:n.1597+2881_1597+2884del
NM_175719.4:c.1597+2881_1597+2884del	NP_783650.1:n.1597+2881_1597+2884del