Canonical Allele Identifier: CA1846095606

Gene: TPM2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35685333T= , CM000671.2:g.35685333T=	GRCh38
NC_000009.11:g.35685330T= , CM000671.1:g.35685330T=	GRCh37
NC_000009.10:g.35675330T=	NCBI36
NG_011620.1:g.9725A= , LRG_680:g.9725A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378292.9:c.499A=	ENSP00000367542.3:p.Arg167=
ENST00000643485.1:n.334A=
ENST00000645482.3:c.499A= MANE Select	ENSP00000496494.2:p.Arg167=
ENST00000647435.1:c.499A=	ENSP00000495440.1:p.Arg167=
ENST00000329305.6:c.499A=	ENSP00000367541.1:p.Arg167=
ENST00000360958.6:c.499A=	ENSP00000354219.2:p.Arg167=
ENST00000378292.7:c.499A=	ENSP00000367542.3:p.Arg167=
ENST00000378300.9:c.499A=	ENSP00000367550.5:p.Arg167=
ENST00000471212.5:n.582A=
ENST00000486018.1:n.117A=
ENST00000604975.1:n.385A=
ENST00000607559.1:c.40A=	ENSP00000475952.1:p.Arg14=
NM_001301226.1:c.499A=	NP_001288155.1:p.Arg167=
NM_001301227.1:c.499A=	NP_001288156.1:p.Arg167=
NM_003289.3:c.499A= , LRG_680t2:c.499A=	NP_003280.2:p.Arg167=
NM_213674.1:c.499A= , LRG_680t1:c.499A=	NP_998839.1:p.Arg167=
XR_929320.1:n.607A=
XR_929321.1:n.607A=
XR_929322.1:n.607A=
XR_929323.1:n.607A=
XR_929324.1:n.610A=
XR_929325.1:n.607A=
XM_017015087.2:c.499A=	XP_016870576.1:p.Arg167=
XM_017015088.2:c.499A=	XP_016870577.1:p.Arg167=
XM_017015090.2:c.499A=	XP_016870579.1:p.Arg167=
XM_017015091.2:c.499A=	XP_016870580.1:p.Arg167=
XM_017015092.2:c.499A=	XP_016870581.1:p.Arg167=
XM_017015093.2:c.499A=	XP_016870582.1:p.Arg167=
NM_001301226.2:c.499A=	NP_001288155.1:p.Arg167=
NM_003289.4:c.499A= MANE Select	NP_003280.2:p.Arg167=
NM_001301227.2:c.499A=	NP_001288156.1:p.Arg167=