Canonical Allele Identifier: CA232647

Gene: TPM2

Linked Data

• ClinVar Variation Id: 140491
• ClinVar RCV Id: RCV001849916 ; RCV000128683
• dbSNP Id: rs199476152
• MyVariant Identifiers: chr9:g.35685525C>G (hg19) ; chr9:g.35685528C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35685528C>G , CM000671.2:g.35685528C>G	GRCh38
NC_000009.11:g.35685525C>G , CM000671.1:g.35685525C>G	GRCh37
NC_000009.10:g.35675525C>G	NCBI36
NG_011620.1:g.9530G>C , LRG_680:g.9530G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378292.9:c.398G>C	ENSP00000367542.3:p.Arg133Pro
ENST00000643485.1:n.233G>C
ENST00000645482.3:c.398G>C MANE Select	ENSP00000496494.2:p.Arg133Pro
ENST00000647435.1:c.398G>C	ENSP00000495440.1:p.Arg133Pro
ENST00000329305.6:c.398G>C	ENSP00000367541.1:p.Arg133Pro
ENST00000360958.6:c.398G>C	ENSP00000354219.2:p.Arg133Pro
ENST00000378292.7:c.398G>C	ENSP00000367542.3:p.Arg133Pro
ENST00000378300.9:c.398G>C	ENSP00000367550.5:p.Arg133Pro
ENST00000471212.5:n.481G>C
ENST00000486018.1:n.16G>C
ENST00000604975.1:n.284G>C
NM_001301226.1:c.398G>C	NP_001288155.1:p.Arg133Pro
NM_001301227.1:c.398G>C	NP_001288156.1:p.Arg133Pro
NM_003289.3:c.398G>C , LRG_680t2:c.398G>C	NP_003280.2:p.Arg133Pro
NM_213674.1:c.398G>C , LRG_680t1:c.398G>C	NP_998839.1:p.Arg133Pro
XR_929320.1:n.506G>C
XR_929321.1:n.506G>C
XR_929322.1:n.506G>C
XR_929323.1:n.506G>C
XR_929324.1:n.509G>C
XR_929325.1:n.506G>C
XM_017015087.2:c.398G>C	XP_016870576.1:p.Arg133Pro
XM_017015088.2:c.398G>C	XP_016870577.1:p.Arg133Pro
XM_017015090.2:c.398G>C	XP_016870579.1:p.Arg133Pro
XM_017015091.2:c.398G>C	XP_016870580.1:p.Arg133Pro
XM_017015092.2:c.398G>C	XP_016870581.1:p.Arg133Pro
XM_017015093.2:c.398G>C	XP_016870582.1:p.Arg133Pro
NM_001301226.2:c.398G>C	NP_001288155.1:p.Arg133Pro
NM_003289.4:c.398G>C MANE Select	NP_003280.2:p.Arg133Pro
NM_001301227.2:c.398G>C	NP_001288156.1:p.Arg133Pro