Canonical Allele Identifier: CA420950078

Gene: TPM3

Linked Data

• gnomAD v4: 1-154191953-C-T
• MyVariant Identifiers: chr1:g.154164429C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154191953C>T , CM000663.2:g.154191953C>T	GRCh38
NC_000001.10:g.154164429C>T , CM000663.1:g.154164429C>T	GRCh37
NC_000001.9:g.152431053C>T	NCBI36
NG_008621.1:g.5181G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368530.7:c.66G>A	ENSP00000357516.3:p.Arg22=
ENST00000651641.1:c.66G>A MANE Select	ENSP00000498577.1:p.Arg22=
ENST00000651644.1:c.66G>A	ENSP00000498648.1:p.Arg22=
ENST00000271850.11:c.66G>A	ENSP00000271850.7:p.Arg22=
ENST00000368530.6:c.66G>A	ENSP00000357516.2:p.Arg22=
ENST00000515609.1:c.66G>A	ENSP00000426306.1:p.Arg22=
NM_152263.3:c.66G>A	NP_689476.2:p.Arg22=
NR_103460.1:n.115G>A
XM_006711515.1:c.66G>A	XP_006711578.1:p.Arg22=
XM_006711517.1:c.66G>A	XP_006711580.1:p.Arg22=
XM_006711518.1:c.66G>A	XP_006711581.1:p.Arg22=
XM_006711519.1:c.66G>A	XP_006711582.1:p.Arg22=
XM_006711520.1:c.66G>A	XP_006711583.1:p.Arg22=
XM_006711521.1:c.66G>A	XP_006711584.1:p.Arg22=
XM_011509950.1:c.66G>A	XP_011508252.1:p.Arg22=
XM_011509951.1:c.66G>A	XP_011508253.1:p.Arg22=
NM_001364679.1:c.66G>A	NP_001351608.1:p.Arg22=
NM_001364680.1:c.66G>A	NP_001351609.1:p.Arg22=
NM_001364681.1:c.66G>A	NP_001351610.1:p.Arg22=
NM_001364682.1:c.66G>A	NP_001351611.1:p.Arg22=
NM_152263.4:c.66G>A MANE Select	NP_689476.2:p.Arg22=
NM_001364679.2:c.66G>A	NP_001351608.1:p.Arg22=
NM_001364680.2:c.66G>A	NP_001351609.1:p.Arg22=
NM_001364681.2:c.66G>A	NP_001351610.1:p.Arg22=
NR_103460.2:n.148G>A