Canonical Allele Identifier: CA1233581685

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1503967C= , CM000664.2:g.1503967C=	GRCh38
NC_000002.11:g.1507739C= , CM000664.1:g.1507739C=	GRCh37
NC_000002.10:g.1486746C=	NCBI36
NG_011581.1:g.95505C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2406C= MANE Select	ENSP00000329869.4:p.Asp802=
ENST00000329066.8:c.2406C=	ENSP00000329869.4:p.Asp802=
ENST00000345913.8:c.2406C=	ENSP00000318820.7:p.Asp802=
ENST00000346956.7:c.2386+7202C=	ENSP00000263886.6:n.2386+7202C=
ENST00000382198.5:c.1887C=	ENSP00000371633.1:p.Asp629=
ENST00000382201.7:c.2235C=	ENSP00000371636.3:p.Asp745=
ENST00000422464.5:c.2173+7202C=	ENSP00000405788.1:n.2173+7202C=
ENST00000425083.3:n.69C=
ENST00000446278.5:c.830C=
ENST00000462973.5:n.424+9928C=
ENST00000469607.3:c.808+7202C=	ENSP00000419461.1:n.808+7202C=
ENST00000497517.6:n.697C=
NM_000547.5:c.2406C=	NP_000538.3:p.Asp802=
NM_001206744.1:c.2406C=	NP_001193673.1:p.Asp802=
NM_001206745.1:c.2235C=	NP_001193674.1:p.Asp745=
NM_175719.3:c.2235C=	NP_783650.1:p.Asp745=
NM_175721.3:c.2386+7202C=	NP_783652.1:n.2386+7202C=
NM_175722.3:c.1887C=	NP_783653.1:p.Asp629=
XM_011510379.1:c.2386+7202C=	XP_011508681.1:n.2386+7202C=
XM_011510380.1:c.2406C=	XP_011508682.1:p.Asp802=
XM_011510381.1:c.2215+7202C=	XP_011508683.1:n.2215+7202C=
XR_922681.1:n.2407C=
XM_011510380.3:c.2442C=	XP_011508682.2:p.Asp814=
XM_024453085.1:c.2422+7202C=	XP_024308853.1:n.2422+7202C=
XM_024453086.1:c.2442C=	XP_024308854.1:p.Asp814=
XM_024453087.1:c.2386+7202C=	XP_024308855.1:n.2386+7202C=
XM_024453088.1:c.2386+7202C=	XP_024308856.1:n.2386+7202C=
XM_024453089.1:c.2386+7202C=	XP_024308857.1:n.2386+7202C=
XM_024453090.1:c.2422+7202C=	XP_024308858.1:n.2422+7202C=
XM_024453091.1:c.2271C=	XP_024308859.1:p.Asp757=
XM_024453092.1:c.2251+7202C=	XP_024308860.1:n.2251+7202C=
XM_024453093.1:c.1923C=	XP_024308861.1:p.Asp641=
NM_001206744.2:c.2406C= MANE Select	NP_001193673.1:p.Asp802=
NM_000547.6:c.2406C=	NP_000538.3:p.Asp802=
NM_001206745.2:c.2235C=	NP_001193674.1:p.Asp745=
NM_175719.4:c.2235C=	NP_783650.1:p.Asp745=