Canonical Allele Identifier: CA342582948

Gene: TPM3

Linked Data

• MyVariant Identifiers: chr1:g.154142938G>T (hg19) ; chr1:g.154170462G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154170462G>T , CM000663.2:g.154170462G>T	GRCh38
NC_000001.10:g.154142938G>T , CM000663.1:g.154142938G>T	GRCh37
NC_000001.9:g.152409562G>T	NCBI36
NG_008621.1:g.26672C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000611659.5:c.539C>A	ENSP00000480520.1:p.Thr180Asn
ENST00000312970.13:n.569C>A
ENST00000323144.12:c.602C>A	ENSP00000357518.4:p.Thr201Asn
ENST00000328159.9:c.602C>A	ENSP00000357520.1:p.Thr201Asn
ENST00000341372.8:c.*318C>A	ENSP00000339378.4:n.*318C>A
ENST00000341485.10:c.602C>A	ENSP00000341653.6:p.Thr201Asn
ENST00000368530.7:c.713C>A	ENSP00000357516.3:p.Thr238Asn
ENST00000368533.8:c.602C>A	ENSP00000357521.3:p.Thr201Asn
ENST00000651641.1:c.713C>A MANE Select	ENSP00000498577.1:p.Thr238Asn
ENST00000651731.1:c.82C>A
ENST00000651873.1:c.623C>A
ENST00000271850.11:c.713C>A	ENSP00000271850.7:p.Thr238Asn
ENST00000302206.9:c.332C>A	ENSP00000307712.5:p.Thr111Asn
ENST00000312970.12:n.492C>A
ENST00000323144.11:c.602C>A	ENSP00000357518.4:p.Thr201Asn
ENST00000328159.8:c.602C>A	ENSP00000357520.1:p.Thr201Asn
ENST00000330188.13:c.602C>A	ENSP00000339035.7:p.Thr201Asn
ENST00000341372.7:c.527C>A	ENSP00000339378.3:p.Thr176Asn
ENST00000341485.9:c.554C>A	ENSP00000341653.5:p.Thr185Asn
ENST00000368530.6:c.713C>A	ENSP00000357516.2:p.Thr238Asn
ENST00000368531.6:c.602C>A	ENSP00000357517.2:p.Thr201Asn
ENST00000368533.7:c.602C>A	ENSP00000357521.3:p.Thr201Asn
ENST00000368545.7:n.720C>A
ENST00000469717.5:n.2616C>A
ENST00000504663.1:n.60C>A
ENST00000509409.5:c.*318C>A	ENSP00000426521.1:n.*318C>A
ENST00000509601.1:c.*112C>A	ENSP00000422207.1:n.*112C>A
ENST00000513769.5:n.287C>A
ENST00000611659.4:c.539C>A	ENSP00000480520.1:p.Thr180Asn
NM_001043351.1:c.602C>A	NP_001036816.1:p.Thr201Asn
NM_001043352.1:c.602C>A	NP_001036817.1:p.Thr201Asn
NM_001043353.1:c.602C>A	NP_001036818.1:p.Thr201Asn
NM_001278188.1:c.404C>A	NP_001265117.1:p.Thr135Asn
NM_001278189.1:c.602C>A	NP_001265118.1:p.Thr201Asn
NM_001278190.1:c.539C>A	NP_001265119.1:p.Thr180Asn
NM_001278191.1:c.332C>A	NP_001265120.1:p.Thr111Asn
NM_152263.3:c.713C>A	NP_689476.2:p.Thr238Asn
NM_153649.3:c.602C>A	NP_705935.1:p.Thr201Asn
NR_103461.1:n.728C>A
XM_006711515.1:c.713C>A	XP_006711578.1:p.Thr238Asn
XM_006711517.1:c.713C>A	XP_006711580.1:p.Thr238Asn
XM_006711518.1:c.713C>A	XP_006711581.1:p.Thr238Asn
XM_006711519.1:c.713C>A	XP_006711582.1:p.Thr238Asn
XM_006711520.1:c.713C>A	XP_006711583.1:p.Thr238Asn
XM_006711521.1:c.713C>A	XP_006711584.1:p.Thr238Asn
XM_006711522.2:c.602C>A	XP_006711585.1:p.Thr201Asn
XM_006711523.2:c.602C>A	XP_006711586.1:p.Thr201Asn
XM_011509950.1:c.713C>A	XP_011508252.1:p.Thr238Asn
XM_011509951.1:c.713C>A	XP_011508253.1:p.Thr238Asn
XM_011509952.1:c.602C>A	XP_011508254.1:p.Thr201Asn
XM_011509953.1:c.602C>A	XP_011508255.1:p.Thr201Asn
XM_011509954.1:c.602C>A	XP_011508256.1:p.Thr201Asn
NM_001349679.1:c.602C>A	NP_001336608.1:p.Thr201Asn
NM_001364679.1:c.713C>A	NP_001351608.1:p.Thr238Asn
NM_001364680.1:c.713C>A	NP_001351609.1:p.Thr238Asn
NM_001364681.1:c.713C>A	NP_001351610.1:p.Thr238Asn
NM_001364682.1:c.713C>A	NP_001351611.1:p.Thr238Asn
NM_001364683.1:c.602C>A	NP_001351612.1:p.Thr201Asn
NM_152263.4:c.713C>A MANE Select	NP_689476.2:p.Thr238Asn
NM_001043351.2:c.602C>A	NP_001036816.1:p.Thr201Asn
NM_001043352.2:c.602C>A	NP_001036817.1:p.Thr201Asn
NM_001043353.2:c.602C>A	NP_001036818.1:p.Thr201Asn
NM_001278188.2:c.404C>A	NP_001265117.1:p.Thr135Asn
NM_001278189.2:c.602C>A	NP_001265118.1:p.Thr201Asn
NM_001278191.2:c.332C>A	NP_001265120.1:p.Thr111Asn
NM_001349679.2:c.602C>A	NP_001336608.1:p.Thr201Asn
NM_001364679.2:c.713C>A	NP_001351608.1:p.Thr238Asn
NM_001364680.2:c.713C>A	NP_001351609.1:p.Thr238Asn
NM_001364681.2:c.713C>A	NP_001351610.1:p.Thr238Asn
NM_153649.4:c.602C>A	NP_705935.1:p.Thr201Asn
NR_103461.2:n.697C>A
NM_001278190.2:c.539C>A	NP_001265119.1:p.Thr180Asn