Canonical Allele Identifier: CA232675

Gene: TPM3

Linked Data

• ClinVar Variation Id: 12446
• ClinVar RCV Id: RCV000013259 ; RCV000128695 ; RCV003151723
• dbSNP Id: rs80358247
• MyVariant Identifiers: chr1:g.154164469A>C (hg19) ; chr1:g.154191993A>C (hg38)
• PubMed: PMID:7663526 ; PMID:7704029 ; PMID:10587521 ; PMID:15562513 ; PMID:20301465

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