Canonical Allele Identifier: CA5047349

Gene: TPM2

Linked Data

• dbSNP Id: rs765401257
• ExAC: 9:35685389 T / C
• gnomAD v2: 9-35685389-T-C
• gnomAD v4: 9-35685392-T-C
• MyVariant Identifiers: chr9:g.35685389T>C (hg19) ; chr9:g.35685392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35685392T>C , CM000671.2:g.35685392T>C	GRCh38
NC_000009.11:g.35685389T>C , CM000671.1:g.35685389T>C	GRCh37
NC_000009.10:g.35675389T>C	NCBI36
NG_011620.1:g.9666A>G , LRG_680:g.9666A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378292.9:c.492+42A>G	ENSP00000367542.3:n.492+42A>G
ENST00000643485.1:n.327+42A>G
ENST00000645482.3:c.492+42A>G MANE Select	ENSP00000496494.2:n.492+42A>G
ENST00000647435.1:c.492+42A>G	ENSP00000495440.1:n.492+42A>G
ENST00000329305.6:c.492+42A>G	ENSP00000367541.1:n.492+42A>G
ENST00000360958.6:c.492+42A>G	ENSP00000354219.2:n.492+42A>G
ENST00000378292.7:c.492+42A>G	ENSP00000367542.3:n.492+42A>G
ENST00000378300.9:c.492+42A>G	ENSP00000367550.5:n.492+42A>G
ENST00000471212.5:n.575+42A>G
ENST00000486018.1:n.110+42A>G
ENST00000604975.1:n.378+42A>G
ENST00000607559.1:c.33+42A>G	ENSP00000475952.1:n.33+42A>G
NM_001301226.1:c.492+42A>G	NP_001288155.1:n.492+42A>G
NM_001301227.1:c.492+42A>G	NP_001288156.1:n.492+42A>G
NM_003289.3:c.492+42A>G , LRG_680t2:c.492+42A>G	NP_003280.2:n.492+42A>G
NM_213674.1:c.492+42A>G , LRG_680t1:c.492+42A>G	NP_998839.1:n.492+42A>G
XR_929320.1:n.600+42A>G
XR_929321.1:n.600+42A>G
XR_929322.1:n.600+42A>G
XR_929323.1:n.600+42A>G
XR_929324.1:n.603+42A>G
XR_929325.1:n.600+42A>G
XM_017015087.2:c.492+42A>G	XP_016870576.1:n.492+42A>G
XM_017015088.2:c.492+42A>G	XP_016870577.1:n.492+42A>G
XM_017015090.2:c.492+42A>G	XP_016870579.1:n.492+42A>G
XM_017015091.2:c.492+42A>G	XP_016870580.1:n.492+42A>G
XM_017015092.2:c.492+42A>G	XP_016870581.1:n.492+42A>G
XM_017015093.2:c.492+42A>G	XP_016870582.1:n.492+42A>G
NM_001301226.2:c.492+42A>G	NP_001288155.1:n.492+42A>G
NM_003289.4:c.492+42A>G MANE Select	NP_003280.2:n.492+42A>G
NM_001301227.2:c.492+42A>G	NP_001288156.1:n.492+42A>G