Canonical Allele Identifier: CA232705

Gene: TPM3

Linked Data

• ClinVar Variation Id: 12449
• ClinVar RCV Id: RCV000013262 ; RCV000128709 ; RCV003764563
• dbSNP Id: rs80358248
• MyVariant Identifiers: chr1:g.154164401G>A (hg19) ; chr1:g.154191925G>A (hg38)
• PubMed: PMID:10619715 ; PMID:18300303 ; PMID:20301465

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154191925G>A , CM000663.2:g.154191925G>A	GRCh38
NC_000001.10:g.154164401G>A , CM000663.1:g.154164401G>A	GRCh37
NC_000001.9:g.152431025G>A	NCBI36
NG_008621.1:g.5209C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368530.7:c.94C>T	ENSP00000357516.3:p.Gln32Ter
ENST00000651641.1:c.94C>T MANE Select	ENSP00000498577.1:p.Gln32Ter
ENST00000651644.1:c.94C>T	ENSP00000498648.1:p.Gln32Ter
ENST00000271850.11:c.94C>T	ENSP00000271850.7:p.Gln32Ter
ENST00000368530.6:c.94C>T	ENSP00000357516.2:p.Gln32Ter
ENST00000466010.1:n.24C>T
ENST00000515609.1:c.94C>T	ENSP00000426306.1:p.Gln32Ter
NM_152263.3:c.94C>T	NP_689476.2:p.Gln32Ter
NR_103460.1:n.143C>T
XM_006711515.1:c.94C>T	XP_006711578.1:p.Gln32Ter
XM_006711517.1:c.94C>T	XP_006711580.1:p.Gln32Ter
XM_006711518.1:c.94C>T	XP_006711581.1:p.Gln32Ter
XM_006711519.1:c.94C>T	XP_006711582.1:p.Gln32Ter
XM_006711520.1:c.94C>T	XP_006711583.1:p.Gln32Ter
XM_006711521.1:c.94C>T	XP_006711584.1:p.Gln32Ter
XM_011509950.1:c.94C>T	XP_011508252.1:p.Gln32Ter
XM_011509951.1:c.94C>T	XP_011508253.1:p.Gln32Ter
NM_001364679.1:c.94C>T	NP_001351608.1:p.Gln32Ter
NM_001364680.1:c.94C>T	NP_001351609.1:p.Gln32Ter
NM_001364681.1:c.94C>T	NP_001351610.1:p.Gln32Ter
NM_001364682.1:c.94C>T	NP_001351611.1:p.Gln32Ter
NM_152263.4:c.94C>T MANE Select	NP_689476.2:p.Gln32Ter
NM_001364679.2:c.94C>T	NP_001351608.1:p.Gln32Ter
NM_001364680.2:c.94C>T	NP_001351609.1:p.Gln32Ter
NM_001364681.2:c.94C>T	NP_001351610.1:p.Gln32Ter
NR_103460.2:n.176C>T