Canonical Allele Identifier: CA1233577885

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1496067_1496069delinsCTG , CM000664.2:g.1496067_1496069delinsCTG	GRCh38
NC_000002.11:g.1499839_1499841delinsCTG , CM000664.1:g.1499839_1499841delinsCTG	GRCh37
NC_000002.10:g.1478846_1478848delinsCTG	NCBI36
NG_011581.1:g.87605_87607delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2085_2087delinsCTG MANE Select	ENSP00000329869.4:p.Ile695=
ENST00000329066.8:c.2085_2087delinsCTG	ENSP00000329869.4:p.Ile695=
ENST00000345913.8:c.2085_2087delinsCTG	ENSP00000318820.7:p.Ile695=
ENST00000346956.7:c.2085_2087delinsCTG	ENSP00000263886.6:p.Ile695=
ENST00000382198.5:c.1566_1568delinsCTG	ENSP00000371633.1:p.Ile522=
ENST00000382201.7:c.1914_1916delinsCTG	ENSP00000371636.3:p.Ile638=
ENST00000422464.5:c.1872_1874delinsCTG	ENSP00000405788.1:p.Ile624=
ENST00000446278.5:c.509_511delinsCTG
ENST00000462973.5:n.424+2028_424+2030delinsCTG
ENST00000469607.3:c.507_509delinsCTG	ENSP00000419461.1:p.Ile169=
ENST00000497517.6:n.677+2028_677+2030delinsCTG
NM_000547.5:c.2085_2087delinsCTG	NP_000538.3:p.Ile695=
NM_001206744.1:c.2085_2087delinsCTG	NP_001193673.1:p.Ile695=
NM_001206745.1:c.1914_1916delinsCTG	NP_001193674.1:p.Ile638=
NM_175719.3:c.1914_1916delinsCTG	NP_783650.1:p.Ile638=
NM_175721.3:c.2085_2087delinsCTG	NP_783652.1:p.Ile695=
NM_175722.3:c.1566_1568delinsCTG	NP_783653.1:p.Ile522=
XM_011510379.1:c.2085_2087delinsCTG	XP_011508681.1:p.Ile695=
XM_011510380.1:c.2085_2087delinsCTG	XP_011508682.1:p.Ile695=
XM_011510381.1:c.1914_1916delinsCTG	XP_011508683.1:p.Ile638=
XR_922681.1:n.2086_2088delinsCTG
XM_011510380.3:c.2121_2123delinsCTG	XP_011508682.2:p.Ile707=
XM_024453085.1:c.2121_2123delinsCTG	XP_024308853.1:p.Ile707=
XM_024453086.1:c.2121_2123delinsCTG	XP_024308854.1:p.Ile707=
XM_024453087.1:c.2085_2087delinsCTG	XP_024308855.1:p.Ile695=
XM_024453088.1:c.2085_2087delinsCTG	XP_024308856.1:p.Ile695=
XM_024453089.1:c.2085_2087delinsCTG	XP_024308857.1:p.Ile695=
XM_024453090.1:c.2121_2123delinsCTG	XP_024308858.1:p.Ile707=
XM_024453091.1:c.1950_1952delinsCTG	XP_024308859.1:p.Ile650=
XM_024453092.1:c.1950_1952delinsCTG	XP_024308860.1:p.Ile650=
XM_024453093.1:c.1602_1604delinsCTG	XP_024308861.1:p.Ile534=
NM_001206744.2:c.2085_2087delinsCTG MANE Select	NP_001193673.1:p.Ile695=
NM_000547.6:c.2085_2087delinsCTG	NP_000538.3:p.Ile695=
NM_001206745.2:c.1914_1916delinsCTG	NP_001193674.1:p.Ile638=
NM_175719.4:c.1914_1916delinsCTG	NP_783650.1:p.Ile638=