Canonical Allele Identifier: CA342587614

Gene: TPM3

Linked Data

• gnomAD v4: 1-154192017-A-G
• MyVariant Identifiers: chr1:g.154164493A>G (hg19) ; chr1:g.154192017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154192017A>G , CM000663.2:g.154192017A>G	GRCh38
NC_000001.10:g.154164493A>G , CM000663.1:g.154164493A>G	GRCh37
NC_000001.9:g.152431117A>G	NCBI36
NG_008621.1:g.5117T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368530.7:c.2T>C	ENSP00000357516.3:p.Met1Thr
ENST00000651641.1:c.2T>C MANE Select	ENSP00000498577.1:p.Met1Thr
ENST00000651644.1:c.2T>C	ENSP00000498648.1:p.Met1Thr
ENST00000271850.11:c.2T>C	ENSP00000271850.7:p.Met1Thr
ENST00000368530.6:c.2T>C	ENSP00000357516.2:p.Met1Thr
ENST00000515609.1:c.2T>C	ENSP00000426306.1:p.Met1Thr
NM_152263.3:c.2T>C	NP_689476.2:p.Met1Thr
NR_103460.1:n.51T>C
XM_006711515.1:c.2T>C	XP_006711578.1:p.Met1Thr
XM_006711517.1:c.2T>C	XP_006711580.1:p.Met1Thr
XM_006711518.1:c.2T>C	XP_006711581.1:p.Met1Thr
XM_006711519.1:c.2T>C	XP_006711582.1:p.Met1Thr
XM_006711520.1:c.2T>C	XP_006711583.1:p.Met1Thr
XM_006711521.1:c.2T>C	XP_006711584.1:p.Met1Thr
XM_011509950.1:c.2T>C	XP_011508252.1:p.Met1Thr
XM_011509951.1:c.2T>C	XP_011508253.1:p.Met1Thr
NM_001364679.1:c.2T>C	NP_001351608.1:p.Met1Thr
NM_001364680.1:c.2T>C	NP_001351609.1:p.Met1Thr
NM_001364681.1:c.2T>C	NP_001351610.1:p.Met1Thr
NM_001364682.1:c.2T>C	NP_001351611.1:p.Met1Thr
NM_152263.4:c.2T>C MANE Select	NP_689476.2:p.Met1Thr
NM_001364679.2:c.2T>C	NP_001351608.1:p.Met1Thr
NM_001364680.2:c.2T>C	NP_001351609.1:p.Met1Thr
NM_001364681.2:c.2T>C	NP_001351610.1:p.Met1Thr
NR_103460.2:n.84T>C