Canonical Allele Identifier: CA2838351788

Gene: TPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.16088124G>T , CM000681.2:g.16088124G>T	GRCh38
NC_000019.9:g.16198934G>T , CM000681.1:g.16198934G>T	GRCh37
NC_000019.8:g.16059934G>T	NCBI36
NG_015841.1:g.25618G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646575.2:c.455+27G>T	ENSP00000496574.2:n.455+27G>T
ENST00000300933.9:c.432+27G>T
ENST00000344824.11:c.185+27G>T	ENSP00000345230.6:n.185+27G>T
ENST00000586193.6:n.549G>T
ENST00000586499.6:c.712+27G>T	ENSP00000468246.2:n.712+27G>T
ENST00000586833.7:c.446+27G>T	ENSP00000467087.3:n.446+27G>T
ENST00000587201.6:n.559G>T
ENST00000588032.6:c.39+27G>T
ENST00000588410.2:n.1081+27G>T
ENST00000588483.2:n.1000+27G>T
ENST00000590180.3:n.479+27G>T
ENST00000592138.6:n.787+27G>T
ENST00000642221.1:c.389+27G>T	ENSP00000495135.1:n.389+27G>T
ENST00000642789.1:c.423+27G>T
ENST00000643494.1:c.455+27G>T	ENSP00000496389.1:n.455+27G>T
ENST00000643579.2:c.455+27G>T MANE Select	ENSP00000495347.1:n.455+27G>T
ENST00000645471.1:c.455+27G>T	ENSP00000494867.1:n.455+27G>T
ENST00000646575.1:c.369+27G>T
ENST00000646974.2:c.563+27G>T	ENSP00000494125.1:n.563+27G>T
ENST00000647037.1:c.455+27G>T	ENSP00000495506.1:n.455+27G>T
ENST00000647464.2:c.455+27G>T	ENSP00000496648.2:n.455+27G>T
ENST00000653979.1:c.271+27G>T
ENST00000655004.1:n.555+27G>T
ENST00000657915.1:n.1115+27G>T
ENST00000658224.1:n.3010+27G>T
ENST00000659595.1:c.*150+27G>T	ENSP00000499765.1:n.*150+27G>T
ENST00000663894.1:n.318+27G>T
ENST00000664983.1:n.692+27G>T
ENST00000668959.1:n.646+27G>T
ENST00000670382.1:c.*513+27G>T	ENSP00000499346.1:n.*513+27G>T
ENST00000300933.8:c.455+27G>T	ENSP00000300933.3:n.455+27G>T
ENST00000344824.10:c.563+27G>T	ENSP00000345230.5:n.563+27G>T
ENST00000586833.5:c.452+27G>T	ENSP00000467087.1:n.452+27G>T
ENST00000587201.5:n.549G>T
ENST00000588032.5:c.39+27G>T
ENST00000588507.5:c.185+27G>T	ENSP00000467558.1:n.185+27G>T
ENST00000592138.5:c.185+27G>T	ENSP00000466654.1:n.185+27G>T
NM_001145160.1:c.563+27G>T	NP_001138632.1:n.563+27G>T
NM_003290.2:c.455+27G>T	NP_003281.1:n.455+27G>T
XM_005260042.2:c.455+27G>T	XP_005260099.1:n.455+27G>T
XM_006722865.1:c.563+27G>T	XP_006722928.1:n.563+27G>T
XM_011528231.1:c.446+27G>T	XP_011526533.1:n.446+27G>T
XM_011528232.1:c.185+27G>T	XP_011526534.1:n.185+27G>T
XM_005260042.4:c.455+27G>T	XP_005260099.1:n.455+27G>T
XM_006722865.2:c.563+27G>T	XP_006722928.1:n.563+27G>T
XM_011528231.2:c.446+27G>T	XP_011526533.1:n.446+27G>T
XM_017027188.1:c.515+27G>T	XP_016882677.1:n.515+27G>T
XM_017027189.1:c.446+27G>T	XP_016882678.1:n.446+27G>T
XM_024451681.1:c.185+27G>T	XP_024307449.1:n.185+27G>T
NM_001145160.2:c.563+27G>T	NP_001138632.1:n.563+27G>T
NM_001367836.1:c.515+27G>T	NP_001354765.1:n.515+27G>T
NM_001367837.1:c.455+27G>T	NP_001354766.1:n.455+27G>T
NM_001367838.1:c.446+27G>T	NP_001354767.1:n.446+27G>T
NM_003290.3:c.455+27G>T MANE Select	NP_003281.1:n.455+27G>T
NM_001367837.2:c.455+27G>T	NP_001354766.1:n.455+27G>T