Canonical Allele Identifier: CA232622
Gene: TPM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12464
ClinVar RCV Id: RCV000013280 RCV000128672 RCV001206319
dbSNP Id: rs137853306
MyVariant Identifiers: chr9:g.35689262C>T (hg19) chr9:g.35689265C>T (hg38)
PubMed: PMID:17846275
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35689265C>T , CM000671.2:g.35689265C>T GRCh38
NC_000009.11:g.35689262C>T , CM000671.1:g.35689262C>T GRCh37
NC_000009.10:g.35679262C>T NCBI36
NG_011620.1:g.5793G>A , LRG_680:g.5793G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378292.9:c.121G>A ENSP00000367542.3:p.Glu41Lys
ENST00000645482.3:c.121G>A MANE Select ENSP00000496494.2:p.Glu41Lys
ENST00000647435.1:c.121G>A ENSP00000495440.1:p.Glu41Lys
ENST00000329305.6:c.121G>A ENSP00000367541.1:p.Glu41Lys
ENST00000360958.6:c.121G>A ENSP00000354219.2:p.Glu41Lys
ENST00000378292.7:c.121G>A ENSP00000367542.3:p.Glu41Lys
ENST00000378300.9:c.121G>A ENSP00000367550.5:p.Glu41Lys
ENST00000471212.5:n.204G>A
ENST00000604975.1:n.222+439G>A
NM_001301226.1:c.121G>A NP_001288155.1:p.Glu41Lys
NM_001301227.1:c.121G>A NP_001288156.1:p.Glu41Lys
NM_003289.3:c.121G>A , LRG_680t2:c.121G>A NP_003280.2:p.Glu41Lys
NM_213674.1:c.121G>A , LRG_680t1:c.121G>A NP_998839.1:p.Glu41Lys
XR_929320.1:n.229G>A
XR_929321.1:n.229G>A
XR_929322.1:n.229G>A
XR_929323.1:n.229G>A
XR_929324.1:n.232G>A
XR_929325.1:n.229G>A
XM_017015087.2:c.121G>A XP_016870576.1:p.Glu41Lys
XM_017015088.2:c.121G>A XP_016870577.1:p.Glu41Lys
XM_017015090.2:c.121G>A XP_016870579.1:p.Glu41Lys
XM_017015091.2:c.121G>A XP_016870580.1:p.Glu41Lys
XM_017015092.2:c.121G>A XP_016870581.1:p.Glu41Lys
XM_017015093.2:c.121G>A XP_016870582.1:p.Glu41Lys
NM_001301226.2:c.121G>A NP_001288155.1:p.Glu41Lys
NM_003289.4:c.121G>A MANE Select NP_003280.2:p.Glu41Lys
NM_001301227.2:c.121G>A NP_001288156.1:p.Glu41Lys
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