Canonical Allele Identifier: CA420950057
Gene: TPM3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154164390T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154191914T>C , CM000663.2:g.154191914T>C GRCh38
NC_000001.10:g.154164390T>C , CM000663.1:g.154164390T>C GRCh37
NC_000001.9:g.152431014T>C NCBI36
NG_008621.1:g.5220A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368530.7:c.105A>G ENSP00000357516.3:p.Glu35=
ENST00000651641.1:c.105A>G MANE Select ENSP00000498577.1:p.Glu35=
ENST00000651644.1:c.105A>G ENSP00000498648.1:p.Glu35=
ENST00000271850.11:c.105A>G ENSP00000271850.7:p.Glu35=
ENST00000368530.6:c.105A>G ENSP00000357516.2:p.Glu35=
ENST00000466010.1:n.35A>G
ENST00000515609.1:c.105A>G ENSP00000426306.1:p.Glu35=
NM_152263.3:c.105A>G NP_689476.2:p.Glu35=
NR_103460.1:n.154A>G
XM_006711515.1:c.105A>G XP_006711578.1:p.Glu35=
XM_006711517.1:c.105A>G XP_006711580.1:p.Glu35=
XM_006711518.1:c.105A>G XP_006711581.1:p.Glu35=
XM_006711519.1:c.105A>G XP_006711582.1:p.Glu35=
XM_006711520.1:c.105A>G XP_006711583.1:p.Glu35=
XM_006711521.1:c.105A>G XP_006711584.1:p.Glu35=
XM_011509950.1:c.105A>G XP_011508252.1:p.Glu35=
XM_011509951.1:c.105A>G XP_011508253.1:p.Glu35=
NM_001364679.1:c.105A>G NP_001351608.1:p.Glu35=
NM_001364680.1:c.105A>G NP_001351609.1:p.Glu35=
NM_001364681.1:c.105A>G NP_001351610.1:p.Glu35=
NM_001364682.1:c.105A>G NP_001351611.1:p.Glu35=
NM_152263.4:c.105A>G MANE Select NP_689476.2:p.Glu35=
NM_001364679.2:c.105A>G NP_001351608.1:p.Glu35=
NM_001364680.2:c.105A>G NP_001351609.1:p.Glu35=
NM_001364681.2:c.105A>G NP_001351610.1:p.Glu35=
NR_103460.2:n.187A>G