Canonical Allele Identifier: CA1233577921

Gene: TPO

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1496155A= , CM000664.2:g.1496155A=	GRCh38
NC_000002.11:g.1499927A= , CM000664.1:g.1499927A=	GRCh37
NC_000002.10:g.1478934A=	NCBI36
NG_011581.1:g.87693A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.2173A= MANE Select	ENSP00000329869.4:p.Thr725=
ENST00000329066.8:c.2173A=	ENSP00000329869.4:p.Thr725=
ENST00000345913.8:c.2173A=	ENSP00000318820.7:p.Thr725=
ENST00000346956.7:c.2173A=	ENSP00000263886.6:p.Thr725=
ENST00000382198.5:c.1654A=	ENSP00000371633.1:p.Thr552=
ENST00000382201.7:c.2002A=	ENSP00000371636.3:p.Thr668=
ENST00000422464.5:c.1960A=	ENSP00000405788.1:p.Thr654=
ENST00000446278.5:c.597A=
ENST00000462973.5:n.424+2116A=
ENST00000469607.3:c.595A=	ENSP00000419461.1:p.Thr199=
ENST00000497517.6:n.677+2116A=
NM_000547.5:c.2173A=	NP_000538.3:p.Thr725=
NM_001206744.1:c.2173A=	NP_001193673.1:p.Thr725=
NM_001206745.1:c.2002A=	NP_001193674.1:p.Thr668=
NM_175719.3:c.2002A=	NP_783650.1:p.Thr668=
NM_175721.3:c.2173A=	NP_783652.1:p.Thr725=
NM_175722.3:c.1654A=	NP_783653.1:p.Thr552=
XM_011510379.1:c.2173A=	XP_011508681.1:p.Thr725=
XM_011510380.1:c.2173A=	XP_011508682.1:p.Thr725=
XM_011510381.1:c.2002A=	XP_011508683.1:p.Thr668=
XR_922681.1:n.2174A=
XM_011510380.3:c.2209A=	XP_011508682.2:p.Thr737=
XM_024453085.1:c.2209A=	XP_024308853.1:p.Thr737=
XM_024453086.1:c.2209A=	XP_024308854.1:p.Thr737=
XM_024453087.1:c.2173A=	XP_024308855.1:p.Thr725=
XM_024453088.1:c.2173A=	XP_024308856.1:p.Thr725=
XM_024453089.1:c.2173A=	XP_024308857.1:p.Thr725=
XM_024453090.1:c.2209A=	XP_024308858.1:p.Thr737=
XM_024453091.1:c.2038A=	XP_024308859.1:p.Thr680=
XM_024453092.1:c.2038A=	XP_024308860.1:p.Thr680=
XM_024453093.1:c.1690A=	XP_024308861.1:p.Thr564=
NM_001206744.2:c.2173A= MANE Select	NP_001193673.1:p.Thr725=
NM_000547.6:c.2173A=	NP_000538.3:p.Thr725=
NM_001206745.2:c.2002A=	NP_001193674.1:p.Thr668=
NM_175719.4:c.2002A=	NP_783650.1:p.Thr668=