Canonical Allele Identifier: CA424502970

Gene: TPO

Linked Data

• gnomAD v4: 2-1484625-G-A
• MyVariant Identifiers: chr2:g.1488397G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1484625G>A , CM000664.2:g.1484625G>A	GRCh38
NC_000002.11:g.1488397G>A , CM000664.1:g.1488397G>A	GRCh37
NC_000002.10:g.1467404G>A	NCBI36
NG_011581.1:g.76163G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000329066.9:c.1368G>A MANE Select	ENSP00000329869.4:p.Arg456=
ENST00000329066.8:c.1368G>A	ENSP00000329869.4:p.Arg456=
ENST00000345913.8:c.1368G>A	ENSP00000318820.7:p.Arg456=
ENST00000346956.7:c.1368G>A	ENSP00000263886.6:p.Arg456=
ENST00000382198.5:c.849G>A	ENSP00000371633.1:p.Arg283=
ENST00000382201.7:c.1368G>A	ENSP00000371636.3:p.Arg456=
ENST00000422464.5:c.1155G>A	ENSP00000405788.1:p.Arg385=
ENST00000497517.6:n.210G>A
NM_000547.5:c.1368G>A	NP_000538.3:p.Arg456=
NM_001206744.1:c.1368G>A	NP_001193673.1:p.Arg456=
NM_001206745.1:c.1368G>A	NP_001193674.1:p.Arg456=
NM_175719.3:c.1368G>A	NP_783650.1:p.Arg456=
NM_175721.3:c.1368G>A	NP_783652.1:p.Arg456=
NM_175722.3:c.849G>A	NP_783653.1:p.Arg283=
XM_011510379.1:c.1368G>A	XP_011508681.1:p.Arg456=
XM_011510380.1:c.1368G>A	XP_011508682.1:p.Arg456=
XM_011510381.1:c.1368G>A	XP_011508683.1:p.Arg456=
XR_922681.1:n.1369G>A
XM_011510380.3:c.1404G>A	XP_011508682.2:p.Arg468=
XM_024453085.1:c.1404G>A	XP_024308853.1:p.Arg468=
XM_024453086.1:c.1404G>A	XP_024308854.1:p.Arg468=
XM_024453087.1:c.1368G>A	XP_024308855.1:p.Arg456=
XM_024453088.1:c.1368G>A	XP_024308856.1:p.Arg456=
XM_024453089.1:c.1368G>A	XP_024308857.1:p.Arg456=
XM_024453090.1:c.1404G>A	XP_024308858.1:p.Arg468=
XM_024453091.1:c.1404G>A	XP_024308859.1:p.Arg468=
XM_024453092.1:c.1404G>A	XP_024308860.1:p.Arg468=
XM_024453093.1:c.885G>A	XP_024308861.1:p.Arg295=
NM_001206744.2:c.1368G>A MANE Select	NP_001193673.1:p.Arg456=
NM_000547.6:c.1368G>A	NP_000538.3:p.Arg456=
NM_001206745.2:c.1368G>A	NP_001193674.1:p.Arg456=
NM_175719.4:c.1368G>A	NP_783650.1:p.Arg456=