Canonical Allele Identifier: CA345695167

Gene: TPO

Linked Data

• gnomAD v4: 2-1484624-G-C
• MyVariant Identifiers: chr2:g.1488396G>C (hg19) ; chr2:g.1484624G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1484624G>C , CM000664.2:g.1484624G>C	GRCh38
NC_000002.11:g.1488396G>C , CM000664.1:g.1488396G>C	GRCh37
NC_000002.10:g.1467403G>C	NCBI36
NG_011581.1:g.76162G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000329066.9:c.1367G>C MANE Select	ENSP00000329869.4:p.Arg456Thr
ENST00000329066.8:c.1367G>C	ENSP00000329869.4:p.Arg456Thr
ENST00000345913.8:c.1367G>C	ENSP00000318820.7:p.Arg456Thr
ENST00000346956.7:c.1367G>C	ENSP00000263886.6:p.Arg456Thr
ENST00000382198.5:c.848G>C	ENSP00000371633.1:p.Arg283Thr
ENST00000382201.7:c.1367G>C	ENSP00000371636.3:p.Arg456Thr
ENST00000422464.5:c.1154G>C	ENSP00000405788.1:p.Arg385Thr
ENST00000497517.6:n.209G>C
NM_000547.5:c.1367G>C	NP_000538.3:p.Arg456Thr
NM_001206744.1:c.1367G>C	NP_001193673.1:p.Arg456Thr
NM_001206745.1:c.1367G>C	NP_001193674.1:p.Arg456Thr
NM_175719.3:c.1367G>C	NP_783650.1:p.Arg456Thr
NM_175721.3:c.1367G>C	NP_783652.1:p.Arg456Thr
NM_175722.3:c.848G>C	NP_783653.1:p.Arg283Thr
XM_011510379.1:c.1367G>C	XP_011508681.1:p.Arg456Thr
XM_011510380.1:c.1367G>C	XP_011508682.1:p.Arg456Thr
XM_011510381.1:c.1367G>C	XP_011508683.1:p.Arg456Thr
XR_922681.1:n.1368G>C
XM_011510380.3:c.1403G>C	XP_011508682.2:p.Arg468Thr
XM_024453085.1:c.1403G>C	XP_024308853.1:p.Arg468Thr
XM_024453086.1:c.1403G>C	XP_024308854.1:p.Arg468Thr
XM_024453087.1:c.1367G>C	XP_024308855.1:p.Arg456Thr
XM_024453088.1:c.1367G>C	XP_024308856.1:p.Arg456Thr
XM_024453089.1:c.1367G>C	XP_024308857.1:p.Arg456Thr
XM_024453090.1:c.1403G>C	XP_024308858.1:p.Arg468Thr
XM_024453091.1:c.1403G>C	XP_024308859.1:p.Arg468Thr
XM_024453092.1:c.1403G>C	XP_024308860.1:p.Arg468Thr
XM_024453093.1:c.884G>C	XP_024308861.1:p.Arg295Thr
NM_001206744.2:c.1367G>C MANE Select	NP_001193673.1:p.Arg456Thr
NM_000547.6:c.1367G>C	NP_000538.3:p.Arg456Thr
NM_001206745.2:c.1367G>C	NP_001193674.1:p.Arg456Thr
NM_175719.4:c.1367G>C	NP_783650.1:p.Arg456Thr