Canonical Allele Identifier: CA2480762985

Gene: TPM3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154191863G= , CM000663.2:g.154191863G=	GRCh38
NC_000001.10:g.154164339G= , CM000663.1:g.154164339G=	GRCh37
NC_000001.9:g.152430963G=	NCBI36
NG_008621.1:g.5271C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368530.7:c.117+39C=	ENSP00000357516.3:n.117+39C=
ENST00000651641.1:c.117+39C= MANE Select	ENSP00000498577.1:n.117+39C=
ENST00000651644.1:c.117+39C=	ENSP00000498648.1:n.117+39C=
ENST00000271850.11:c.117+39C=	ENSP00000271850.7:n.117+39C=
ENST00000368530.6:c.117+39C=	ENSP00000357516.2:n.117+39C=
ENST00000466010.1:n.47+39C=
ENST00000515609.1:c.117+39C=	ENSP00000426306.1:n.117+39C=
NM_152263.3:c.117+39C=	NP_689476.2:n.117+39C=
NR_103460.1:n.166+39C=
XM_006711515.1:c.117+39C=	XP_006711578.1:n.117+39C=
XM_006711517.1:c.117+39C=	XP_006711580.1:n.117+39C=
XM_006711518.1:c.117+39C=	XP_006711581.1:n.117+39C=
XM_006711519.1:c.117+39C=	XP_006711582.1:n.117+39C=
XM_006711520.1:c.117+39C=	XP_006711583.1:n.117+39C=
XM_006711521.1:c.117+39C=	XP_006711584.1:n.117+39C=
XM_011509950.1:c.117+39C=	XP_011508252.1:n.117+39C=
XM_011509951.1:c.117+39C=	XP_011508253.1:n.117+39C=
NM_001364679.1:c.117+39C=	NP_001351608.1:n.117+39C=
NM_001364680.1:c.117+39C=	NP_001351609.1:n.117+39C=
NM_001364681.1:c.117+39C=	NP_001351610.1:n.117+39C=
NM_001364682.1:c.117+39C=	NP_001351611.1:n.117+39C=
NM_152263.4:c.117+39C= MANE Select	NP_689476.2:n.117+39C=
NM_001364679.2:c.117+39C=	NP_001351608.1:n.117+39C=
NM_001364680.2:c.117+39C=	NP_001351609.1:n.117+39C=
NM_001364681.2:c.117+39C=	NP_001351610.1:n.117+39C=
NR_103460.2:n.199+39C=