Canonical Allele Identifier: CA342587588

Gene: TPM3

Linked Data

• gnomAD v4: 1-154192008-G-T
• MyVariant Identifiers: chr1:g.154164484G>T (hg19) ; chr1:g.154192008G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154192008G>T , CM000663.2:g.154192008G>T	GRCh38
NC_000001.10:g.154164484G>T , CM000663.1:g.154164484G>T	GRCh37
NC_000001.9:g.152431108G>T	NCBI36
NG_008621.1:g.5126C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368530.7:c.11C>A	ENSP00000357516.3:p.Ala4Asp
ENST00000651641.1:c.11C>A MANE Select	ENSP00000498577.1:p.Ala4Asp
ENST00000651644.1:c.11C>A	ENSP00000498648.1:p.Ala4Asp
ENST00000271850.11:c.11C>A	ENSP00000271850.7:p.Ala4Asp
ENST00000368530.6:c.11C>A	ENSP00000357516.2:p.Ala4Asp
ENST00000515609.1:c.11C>A	ENSP00000426306.1:p.Ala4Asp
NM_152263.3:c.11C>A	NP_689476.2:p.Ala4Asp
NR_103460.1:n.60C>A
XM_006711515.1:c.11C>A	XP_006711578.1:p.Ala4Asp
XM_006711517.1:c.11C>A	XP_006711580.1:p.Ala4Asp
XM_006711518.1:c.11C>A	XP_006711581.1:p.Ala4Asp
XM_006711519.1:c.11C>A	XP_006711582.1:p.Ala4Asp
XM_006711520.1:c.11C>A	XP_006711583.1:p.Ala4Asp
XM_006711521.1:c.11C>A	XP_006711584.1:p.Ala4Asp
XM_011509950.1:c.11C>A	XP_011508252.1:p.Ala4Asp
XM_011509951.1:c.11C>A	XP_011508253.1:p.Ala4Asp
NM_001364679.1:c.11C>A	NP_001351608.1:p.Ala4Asp
NM_001364680.1:c.11C>A	NP_001351609.1:p.Ala4Asp
NM_001364681.1:c.11C>A	NP_001351610.1:p.Ala4Asp
NM_001364682.1:c.11C>A	NP_001351611.1:p.Ala4Asp
NM_152263.4:c.11C>A MANE Select	NP_689476.2:p.Ala4Asp
NM_001364679.2:c.11C>A	NP_001351608.1:p.Ala4Asp
NM_001364680.2:c.11C>A	NP_001351609.1:p.Ala4Asp
NM_001364681.2:c.11C>A	NP_001351610.1:p.Ala4Asp
NR_103460.2:n.93C>A