Canonical Allele Identifier: CA1125826

Gene: TPM3

Linked Data

• dbSNP Id: rs749012587
• ExAC: 1:154164372 GCCTA / G
• gnomAD v2: 1-154164372-GCCTA-G
• gnomAD v3: 1-154191896-GCCTA-G
• gnomAD v4: 1-154191896-GCCTA-G
• MyVariant Identifiers: chr1:g.154164373_154164376del (hg19) ; chr1:g.154191897_154191900del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154191900_154191903del , CM000663.2:g.154191900_154191903del	GRCh38
NC_000001.10:g.154164376_154164379del , CM000663.1:g.154164376_154164379del	GRCh37
NC_000001.9:g.152431000_152431003del	NCBI36
NG_008621.1:g.5234_5237del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368530.7:c.117+2_117+5del
ENST00000651641.1:c.117+2_117+5del
ENST00000651644.1:c.117+2_117+5del
ENST00000271850.11:c.117+2_117+5del
ENST00000368530.6:c.117+2_117+5del
ENST00000466010.1:n.47+2_47+5del
ENST00000515609.1:c.117+2_117+5del
NM_152263.3:c.117+2_117+5del
NR_103460.1:n.166+2_166+5del
XM_006711515.1:c.117+2_117+5del
XM_006711517.1:c.117+2_117+5del
XM_006711518.1:c.117+2_117+5del
XM_006711519.1:c.117+2_117+5del
XM_006711520.1:c.117+2_117+5del
XM_006711521.1:c.117+2_117+5del
XM_011509950.1:c.117+2_117+5del
XM_011509951.1:c.117+2_117+5del
NM_001364679.1:c.117+2_117+5del
NM_001364680.1:c.117+2_117+5del
NM_001364681.1:c.117+2_117+5del
NM_001364682.1:c.117+2_117+5del
NM_152263.4:c.117+2_117+5del
NM_001364679.2:c.117+2_117+5del
NM_001364680.2:c.117+2_117+5del
NM_001364681.2:c.117+2_117+5del
NR_103460.2:n.199+2_199+5del