Canonical Allele Identifier: CA122403
Gene: TPM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12460
dbSNP Id: rs104894127

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35685750G>C , CM000671.2:g.35685750G>C GRCh38
NC_000009.11:g.35685747G>C , CM000671.1:g.35685747G>C GRCh37
NC_000009.10:g.35675747G>C NCBI36
NG_011620.1:g.9308C>G , LRG_680:g.9308C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378292.9:c.271C>G ENSP00000367542.3:p.Arg91Gly
ENST00000643485.1:n.106C>G
ENST00000645482.3:c.271C>G MANE Select ENSP00000496494.2:p.Arg91Gly
ENST00000647435.1:c.271C>G ENSP00000495440.1:p.Arg91Gly
ENST00000329305.6:c.271C>G ENSP00000367541.1:p.Arg91Gly
ENST00000360958.6:c.271C>G ENSP00000354219.2:p.Arg91Gly
ENST00000378292.7:c.271C>G ENSP00000367542.3:p.Arg91Gly
ENST00000378300.9:c.271C>G ENSP00000367550.5:p.Arg91Gly
ENST00000471212.5:n.354C>G
ENST00000604975.1:n.223-66C>G
NM_001301226.1:c.271C>G NP_001288155.1:p.Arg91Gly
NM_001301227.1:c.271C>G NP_001288156.1:p.Arg91Gly
NM_003289.3:c.271C>G , LRG_680t2:c.271C>G NP_003280.2:p.Arg91Gly
NM_213674.1:c.271C>G , LRG_680t1:c.271C>G NP_998839.1:p.Arg91Gly
XR_929320.1:n.379C>G
XR_929321.1:n.379C>G
XR_929322.1:n.379C>G
XR_929323.1:n.379C>G
XR_929324.1:n.382C>G
XR_929325.1:n.379C>G
XM_017015087.2:c.271C>G XP_016870576.1:p.Arg91Gly
XM_017015088.2:c.271C>G XP_016870577.1:p.Arg91Gly
XM_017015090.2:c.271C>G XP_016870579.1:p.Arg91Gly
XM_017015091.2:c.271C>G XP_016870580.1:p.Arg91Gly
XM_017015092.2:c.271C>G XP_016870581.1:p.Arg91Gly
XM_017015093.2:c.271C>G XP_016870582.1:p.Arg91Gly
NM_001301226.2:c.271C>G NP_001288155.1:p.Arg91Gly
NM_003289.4:c.271C>G MANE Select NP_003280.2:p.Arg91Gly
NM_001301227.2:c.271C>G NP_001288156.1:p.Arg91Gly