Canonical Allele Identifier: CA1846095858
Gene: TPM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35685446G= , CM000671.2:g.35685446G= GRCh38
NC_000009.11:g.35685443G= , CM000671.1:g.35685443G= GRCh37
NC_000009.10:g.35675443G= NCBI36
NG_011620.1:g.9612C= , LRG_680:g.9612C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378292.9:c.480C= ENSP00000367542.3:p.Arg160=
ENST00000643485.1:n.315C=
ENST00000645482.3:c.480C= MANE Select ENSP00000496494.2:p.Arg160=
ENST00000647435.1:c.480C= ENSP00000495440.1:p.Arg160=
ENST00000329305.6:c.480C= ENSP00000367541.1:p.Arg160=
ENST00000360958.6:c.480C= ENSP00000354219.2:p.Arg160=
ENST00000378292.7:c.480C= ENSP00000367542.3:p.Arg160=
ENST00000378300.9:c.480C= ENSP00000367550.5:p.Arg160=
ENST00000471212.5:n.563C=
ENST00000486018.1:n.98C=
ENST00000604975.1:n.366C=
ENST00000607559.1:c.21C= ENSP00000475952.1:p.Arg7=
NM_001301226.1:c.480C= NP_001288155.1:p.Arg160=
NM_001301227.1:c.480C= NP_001288156.1:p.Arg160=
NM_003289.3:c.480C= , LRG_680t2:c.480C= NP_003280.2:p.Arg160=
NM_213674.1:c.480C= , LRG_680t1:c.480C= NP_998839.1:p.Arg160=
XR_929320.1:n.588C=
XR_929321.1:n.588C=
XR_929322.1:n.588C=
XR_929323.1:n.588C=
XR_929324.1:n.591C=
XR_929325.1:n.588C=
XM_017015087.2:c.480C= XP_016870576.1:p.Arg160=
XM_017015088.2:c.480C= XP_016870577.1:p.Arg160=
XM_017015090.2:c.480C= XP_016870579.1:p.Arg160=
XM_017015091.2:c.480C= XP_016870580.1:p.Arg160=
XM_017015092.2:c.480C= XP_016870581.1:p.Arg160=
XM_017015093.2:c.480C= XP_016870582.1:p.Arg160=
NM_001301226.2:c.480C= NP_001288155.1:p.Arg160=
NM_003289.4:c.480C= MANE Select NP_003280.2:p.Arg160=
NM_001301227.2:c.480C= NP_001288156.1:p.Arg160=