Canonical Allele Identifier: CA1233577881

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1496059C= , CM000664.2:g.1496059C=	GRCh38
NC_000002.11:g.1499831C= , CM000664.1:g.1499831C=	GRCh37
NC_000002.10:g.1478838C=	NCBI36
NG_011581.1:g.87597C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001206744.2:c.2077C= MANE Select	NP_001193673.1:p.Arg693=
ENST00000329066.9:c.2077C= MANE Select	ENSP00000329869.4:p.Arg693=
NM_000547.5:c.2077C=	NP_000538.3:p.Arg693=
NM_000547.6:c.2077C=	NP_000538.3:p.Arg693=
NM_001206744.1:c.2077C=	NP_001193673.1:p.Arg693=
NM_001206745.1:c.1906C=	NP_001193674.1:p.Arg636=
NM_001206745.2:c.1906C=	NP_001193674.1:p.Arg636=
NM_175719.3:c.1906C=	NP_783650.1:p.Arg636=
NM_175719.4:c.1906C=	NP_783650.1:p.Arg636=
NM_175721.3:c.2077C=	NP_783652.1:p.Arg693=
NM_175722.3:c.1558C=	NP_783653.1:p.Arg520=
ENST00000329066.8:c.2077C=	ENSP00000329869.4:p.Arg693=
ENST00000345913.8:c.2077C=	ENSP00000318820.7:p.Arg693=
ENST00000346956.7:c.2077C=	ENSP00000263886.6:p.Arg693=
ENST00000382198.5:c.1558C=	ENSP00000371633.1:p.Arg520=
ENST00000382201.7:c.1906C=	ENSP00000371636.3:p.Arg636=
ENST00000422464.5:c.1864C=	ENSP00000405788.1:p.Arg622=
ENST00000446278.5:c.501C=
ENST00000462973.5:n.424+2020C=
ENST00000469607.3:c.499C=	ENSP00000419461.1:p.Arg167=
ENST00000497517.6:n.677+2020C=
XM_011510379.1:c.2077C=	XP_011508681.1:p.Arg693=
XM_011510380.1:c.2077C=	XP_011508682.1:p.Arg693=
XM_011510380.3:c.2113C=	XP_011508682.2:p.Arg705=
XM_011510381.1:c.1906C=	XP_011508683.1:p.Arg636=
XM_024453085.1:c.2113C=	XP_024308853.1:p.Arg705=
XM_024453086.1:c.2113C=	XP_024308854.1:p.Arg705=
XM_024453087.1:c.2077C=	XP_024308855.1:p.Arg693=
XM_024453088.1:c.2077C=	XP_024308856.1:p.Arg693=
XM_024453089.1:c.2077C=	XP_024308857.1:p.Arg693=
XM_024453090.1:c.2113C=	XP_024308858.1:p.Arg705=
XM_024453091.1:c.1942C=	XP_024308859.1:p.Arg648=
XM_024453092.1:c.1942C=	XP_024308860.1:p.Arg648=
XM_024453093.1:c.1594C=	XP_024308861.1:p.Arg532=
XR_922681.1:n.2078C=