Canonical Allele Identifier: CA1125838

Gene: TPM3

Linked Data

• dbSNP Id: rs773857288
• ExAC: 1:154164501 T / C
• gnomAD v2: 1-154164501-T-C
• gnomAD v4: 1-154192025-T-C
• MyVariant Identifiers: chr1:g.154164501T>C (hg19) ; chr1:g.154192025T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154192025T>C , CM000663.2:g.154192025T>C	GRCh38
NC_000001.10:g.154164501T>C , CM000663.1:g.154164501T>C	GRCh37
NC_000001.9:g.152431125T>C	NCBI36
NG_008621.1:g.5109A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368530.7:c.-7A>G	ENSP00000357516.3:n.-7A>G
ENST00000651641.1:c.-7A>G MANE Select	ENSP00000498577.1:n.-7A>G
ENST00000651644.1:c.-7A>G	ENSP00000498648.1:n.-7A>G
ENST00000271850.11:c.-7A>G	ENSP00000271850.7:n.-7A>G
ENST00000368530.6:c.-7A>G	ENSP00000357516.2:n.-7A>G
ENST00000515609.1:c.-7A>G	ENSP00000426306.1:n.-7A>G
NM_152263.3:c.-7A>G	NP_689476.2:n.-7A>G
NR_103460.1:n.43A>G
XM_006711515.1:c.-7A>G	XP_006711578.1:n.-7A>G
XM_006711517.1:c.-7A>G	XP_006711580.1:n.-7A>G
XM_006711518.1:c.-7A>G	XP_006711581.1:n.-7A>G
XM_006711519.1:c.-7A>G	XP_006711582.1:n.-7A>G
XM_006711520.1:c.-7A>G	XP_006711583.1:n.-7A>G
XM_006711521.1:c.-7A>G	XP_006711584.1:n.-7A>G
XM_011509950.1:c.-7A>G	XP_011508252.1:n.-7A>G
XM_011509951.1:c.-7A>G	XP_011508253.1:n.-7A>G
NM_001364679.1:c.-7A>G	NP_001351608.1:n.-7A>G
NM_001364680.1:c.-7A>G	NP_001351609.1:n.-7A>G
NM_001364681.1:c.-7A>G	NP_001351610.1:n.-7A>G
NM_001364682.1:c.-7A>G	NP_001351611.1:n.-7A>G
NM_152263.4:c.-7A>G MANE Select	NP_689476.2:n.-7A>G
NM_001364679.2:c.-7A>G	NP_001351608.1:n.-7A>G
NM_001364680.2:c.-7A>G	NP_001351609.1:n.-7A>G
NM_001364681.2:c.-7A>G	NP_001351610.1:n.-7A>G
NR_103460.2:n.76A>G