Canonical Allele Identifier: CA342584178

Gene: TPM3

Linked Data

• MyVariant Identifiers: chr1:g.154145424C>A (hg19) ; chr1:g.154172948C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154172948C>A , CM000663.2:g.154172948C>A	GRCh38
NC_000001.10:g.154145424C>A , CM000663.1:g.154145424C>A	GRCh37
NC_000001.9:g.152412048C>A	NCBI36
NG_008621.1:g.24186G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000611659.5:c.415G>T	ENSP00000480520.1:p.Asp139Tyr
ENST00000312970.13:n.382G>T
ENST00000323144.12:c.415G>T	ENSP00000357518.4:p.Asp139Tyr
ENST00000328159.9:c.415G>T	ENSP00000357520.1:p.Asp139Tyr
ENST00000341372.8:c.*131G>T	ENSP00000339378.4:n.*131G>T
ENST00000341485.10:c.415G>T	ENSP00000341653.6:p.Asp139Tyr
ENST00000368530.7:c.526G>T	ENSP00000357516.3:p.Asp176Tyr
ENST00000368533.8:c.415G>T	ENSP00000357521.3:p.Asp139Tyr
ENST00000651641.1:c.526G>T MANE Select	ENSP00000498577.1:p.Asp176Tyr
ENST00000651644.1:c.526G>T	ENSP00000498648.1:p.Asp176Tyr
ENST00000651873.1:c.436G>T
ENST00000271850.11:c.526G>T	ENSP00000271850.7:p.Asp176Tyr
ENST00000302206.9:c.145G>T	ENSP00000307712.5:p.Asp49Tyr
ENST00000312970.12:n.305G>T
ENST00000323144.11:c.415G>T	ENSP00000357518.4:p.Asp139Tyr
ENST00000328159.8:c.415G>T	ENSP00000357520.1:p.Asp139Tyr
ENST00000330188.13:c.415G>T	ENSP00000339035.7:p.Asp139Tyr
ENST00000341372.7:c.340G>T	ENSP00000339378.3:p.Asp114Tyr
ENST00000341485.9:c.367G>T	ENSP00000341653.5:p.Asp123Tyr
ENST00000368527.7:n.491G>T
ENST00000368530.6:c.526G>T	ENSP00000357516.2:p.Asp176Tyr
ENST00000368531.6:c.415G>T	ENSP00000357517.2:p.Asp139Tyr
ENST00000368533.7:c.415G>T	ENSP00000357521.3:p.Asp139Tyr
ENST00000469717.5:n.309G>T
ENST00000473036.2:n.470G>T
ENST00000505010.5:n.277G>T
ENST00000509409.5:c.*131G>T	ENSP00000426521.1:n.*131G>T
ENST00000509601.1:c.267-857G>T	ENSP00000422207.1:n.267-857G>T
ENST00000611659.4:c.415G>T	ENSP00000480520.1:p.Asp139Tyr
NM_001043351.1:c.415G>T	NP_001036816.1:p.Asp139Tyr
NM_001043352.1:c.415G>T	NP_001036817.1:p.Asp139Tyr
NM_001043353.1:c.415G>T	NP_001036818.1:p.Asp139Tyr
NM_001278188.1:c.217G>T	NP_001265117.1:p.Asp73Tyr
NM_001278189.1:c.415G>T	NP_001265118.1:p.Asp139Tyr
NM_001278190.1:c.415G>T	NP_001265119.1:p.Asp139Tyr
NM_001278191.1:c.145G>T	NP_001265120.1:p.Asp49Tyr
NM_152263.3:c.526G>T	NP_689476.2:p.Asp176Tyr
NM_153649.3:c.415G>T	NP_705935.1:p.Asp139Tyr
NR_103461.1:n.545G>T
XM_006711515.1:c.526G>T	XP_006711578.1:p.Asp176Tyr
XM_006711517.1:c.526G>T	XP_006711580.1:p.Asp176Tyr
XM_006711518.1:c.526G>T	XP_006711581.1:p.Asp176Tyr
XM_006711519.1:c.526G>T	XP_006711582.1:p.Asp176Tyr
XM_006711520.1:c.526G>T	XP_006711583.1:p.Asp176Tyr
XM_006711521.1:c.526G>T	XP_006711584.1:p.Asp176Tyr
XM_006711522.2:c.415G>T	XP_006711585.1:p.Asp139Tyr
XM_006711523.2:c.415G>T	XP_006711586.1:p.Asp139Tyr
XM_011509950.1:c.526G>T	XP_011508252.1:p.Asp176Tyr
XM_011509951.1:c.526G>T	XP_011508253.1:p.Asp176Tyr
XM_011509952.1:c.415G>T	XP_011508254.1:p.Asp139Tyr
XM_011509953.1:c.415G>T	XP_011508255.1:p.Asp139Tyr
XM_011509954.1:c.415G>T	XP_011508256.1:p.Asp139Tyr
NM_001349679.1:c.415G>T	NP_001336608.1:p.Asp139Tyr
NM_001364679.1:c.526G>T	NP_001351608.1:p.Asp176Tyr
NM_001364680.1:c.526G>T	NP_001351609.1:p.Asp176Tyr
NM_001364681.1:c.526G>T	NP_001351610.1:p.Asp176Tyr
NM_001364682.1:c.526G>T	NP_001351611.1:p.Asp176Tyr
NM_001364683.1:c.415G>T	NP_001351612.1:p.Asp139Tyr
NM_152263.4:c.526G>T MANE Select	NP_689476.2:p.Asp176Tyr
NM_001043351.2:c.415G>T	NP_001036816.1:p.Asp139Tyr
NM_001043352.2:c.415G>T	NP_001036817.1:p.Asp139Tyr
NM_001043353.2:c.415G>T	NP_001036818.1:p.Asp139Tyr
NM_001278188.2:c.217G>T	NP_001265117.1:p.Asp73Tyr
NM_001278189.2:c.415G>T	NP_001265118.1:p.Asp139Tyr
NM_001278191.2:c.145G>T	NP_001265120.1:p.Asp49Tyr
NM_001349679.2:c.415G>T	NP_001336608.1:p.Asp139Tyr
NM_001364679.2:c.526G>T	NP_001351608.1:p.Asp176Tyr
NM_001364680.2:c.526G>T	NP_001351609.1:p.Asp176Tyr
NM_001364681.2:c.526G>T	NP_001351610.1:p.Asp176Tyr
NM_153649.4:c.415G>T	NP_705935.1:p.Asp139Tyr
NR_103461.2:n.514G>T
NM_001278190.2:c.415G>T	NP_001265119.1:p.Asp139Tyr