Canonical Allele Identifier: CA232675
Gene: TPM3 HGNC NCBI

Linked Data

ClinVar Variation Id: 12446
dbSNP Id: rs80358247

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154191993A>C , CM000663.2:g.154191993A>C GRCh38
NC_000001.10:g.154164469A>C , CM000663.1:g.154164469A>C GRCh37
NC_000001.9:g.152431093A>C NCBI36
NG_008621.1:g.5141T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368530.7:c.26T>G ENSP00000357516.3:p.Met9Arg
ENST00000651641.1:c.26T>G MANE Select ENSP00000498577.1:p.Met9Arg
ENST00000651644.1:c.26T>G ENSP00000498648.1:p.Met9Arg
ENST00000271850.11:c.26T>G ENSP00000271850.7:p.Met9Arg
ENST00000368530.6:c.26T>G ENSP00000357516.2:p.Met9Arg
ENST00000515609.1:c.26T>G ENSP00000426306.1:p.Met9Arg
NM_152263.3:c.26T>G NP_689476.2:p.Met9Arg
NR_103460.1:n.75T>G
XM_006711515.1:c.26T>G XP_006711578.1:p.Met9Arg
XM_006711517.1:c.26T>G XP_006711580.1:p.Met9Arg
XM_006711518.1:c.26T>G XP_006711581.1:p.Met9Arg
XM_006711519.1:c.26T>G XP_006711582.1:p.Met9Arg
XM_006711520.1:c.26T>G XP_006711583.1:p.Met9Arg
XM_006711521.1:c.26T>G XP_006711584.1:p.Met9Arg
XM_011509950.1:c.26T>G XP_011508252.1:p.Met9Arg
XM_011509951.1:c.26T>G XP_011508253.1:p.Met9Arg
NM_001364679.1:c.26T>G NP_001351608.1:p.Met9Arg
NM_001364680.1:c.26T>G NP_001351609.1:p.Met9Arg
NM_001364681.1:c.26T>G NP_001351610.1:p.Met9Arg
NM_001364682.1:c.26T>G NP_001351611.1:p.Met9Arg
NM_152263.4:c.26T>G MANE Select NP_689476.2:p.Met9Arg
NM_001364679.2:c.26T>G NP_001351608.1:p.Met9Arg
NM_001364680.2:c.26T>G NP_001351609.1:p.Met9Arg
NM_001364681.2:c.26T>G NP_001351610.1:p.Met9Arg
NR_103460.2:n.108T>G