Canonical Allele Identifier: CA2657646527

Gene: TPO

Linked Data

• gnomAD v4: 2-1488062-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1488068_1488069del , CM000664.2:g.1488068_1488069del	GRCh38
NC_000002.11:g.1491840_1491841del , CM000664.1:g.1491840_1491841del	GRCh37
NC_000002.10:g.1470847_1470848del	NCBI36
NG_011581.1:g.79606_79607del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.1768+77_1768+78del MANE Select	ENSP00000329869.4:n.1768+77_1768+78del
ENST00000329066.8:c.1768+77_1768+78del	ENSP00000329869.4:n.1768+77_1768+78del
ENST00000345913.8:c.1768+77_1768+78del	ENSP00000318820.7:n.1768+77_1768+78del
ENST00000346956.7:c.1768+77_1768+78del	ENSP00000263886.6:n.1768+77_1768+78del
ENST00000382198.5:c.1249+77_1249+78del	ENSP00000371633.1:n.1249+77_1249+78del
ENST00000382201.7:c.1597+3214_1597+3215del	ENSP00000371636.3:n.1597+3214_1597+3215del
ENST00000422464.5:c.1555+77_1555+78del	ENSP00000405788.1:n.1555+77_1555+78del
ENST00000446278.5:c.192+3214_192+3215del
ENST00000462973.5:n.186+3214_186+3215del
ENST00000469607.3:c.190+3214_190+3215del	ENSP00000419461.1:n.190+3214_190+3215del
ENST00000497517.6:n.439+3214_439+3215del
NM_000547.5:c.1768+77_1768+78del	NP_000538.3:n.1768+77_1768+78del
NM_001206744.1:c.1768+77_1768+78del	NP_001193673.1:n.1768+77_1768+78del
NM_001206745.1:c.1597+3214_1597+3215del	NP_001193674.1:n.1597+3214_1597+3215del
NM_175719.3:c.1597+3214_1597+3215del	NP_783650.1:n.1597+3214_1597+3215del
NM_175721.3:c.1768+77_1768+78del	NP_783652.1:n.1768+77_1768+78del
NM_175722.3:c.1249+77_1249+78del	NP_783653.1:n.1249+77_1249+78del
XM_011510379.1:c.1768+77_1768+78del	XP_011508681.1:n.1768+77_1768+78del
XM_011510380.1:c.1768+77_1768+78del	XP_011508682.1:n.1768+77_1768+78del
XM_011510381.1:c.1597+3214_1597+3215del	XP_011508683.1:n.1597+3214_1597+3215del
XR_922681.1:n.1769+77_1769+78del
XM_011510380.3:c.1804+77_1804+78del	XP_011508682.2:n.1804+77_1804+78del
XM_024453085.1:c.1804+77_1804+78del	XP_024308853.1:n.1804+77_1804+78del
XM_024453086.1:c.1804+77_1804+78del	XP_024308854.1:n.1804+77_1804+78del
XM_024453087.1:c.1768+77_1768+78del	XP_024308855.1:n.1768+77_1768+78del
XM_024453088.1:c.1768+77_1768+78del	XP_024308856.1:n.1768+77_1768+78del
XM_024453089.1:c.1768+77_1768+78del	XP_024308857.1:n.1768+77_1768+78del
XM_024453090.1:c.1804+77_1804+78del	XP_024308858.1:n.1804+77_1804+78del
XM_024453091.1:c.1633+3214_1633+3215del	XP_024308859.1:n.1633+3214_1633+3215del
XM_024453092.1:c.1633+3214_1633+3215del	XP_024308860.1:n.1633+3214_1633+3215del
XM_024453093.1:c.1285+77_1285+78del	XP_024308861.1:n.1285+77_1285+78del
NM_001206744.2:c.1768+77_1768+78del MANE Select	NP_001193673.1:n.1768+77_1768+78del
NM_000547.6:c.1768+77_1768+78del	NP_000538.3:n.1768+77_1768+78del
NM_001206745.2:c.1597+3214_1597+3215del	NP_001193674.1:n.1597+3214_1597+3215del
NM_175719.4:c.1597+3214_1597+3215del	NP_783650.1:n.1597+3214_1597+3215del