Canonical Allele Identifier: CA863584470

Gene: TPM2

Linked Data

• dbSNP Id: rs1485264928
• gnomAD v3: 9-35689558-GGCCCT-G
• gnomAD v4: 9-35689558-GGCCCT-G
• MyVariant Identifiers: chr9:g.35689556_35689560del (hg19) ; chr9:g.35689559_35689563del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35689560_35689564del , CM000671.2:g.35689560_35689564del	GRCh38
NC_000009.11:g.35689557_35689561del , CM000671.1:g.35689557_35689561del	GRCh37
NC_000009.10:g.35679557_35679561del	NCBI36
NG_011620.1:g.5495_5499del , LRG_680:g.5495_5499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378292.9:c.114+141_114+145del	ENSP00000367542.3:n.114+141_114+145del
ENST00000645482.3:c.114+141_114+145del MANE Select	ENSP00000496494.2:n.114+141_114+145del
ENST00000647435.1:c.114+141_114+145del	ENSP00000495440.1:n.114+141_114+145del
ENST00000329305.6:c.114+141_114+145del	ENSP00000367541.1:n.114+141_114+145del
ENST00000360958.6:c.114+141_114+145del	ENSP00000354219.2:n.114+141_114+145del
ENST00000378292.7:c.114+141_114+145del	ENSP00000367542.3:n.114+141_114+145del
ENST00000378300.9:c.114+141_114+145del	ENSP00000367550.5:n.114+141_114+145del
ENST00000471212.5:n.197+141_197+145del
ENST00000604975.1:n.222+141_222+145del
NM_001301226.1:c.114+141_114+145del	NP_001288155.1:n.114+141_114+145del
NM_001301227.1:c.114+141_114+145del	NP_001288156.1:n.114+141_114+145del
NM_003289.3:c.114+141_114+145del , LRG_680t2:c.114+141_114+145del	NP_003280.2:n.114+141_114+145del
NM_213674.1:c.114+141_114+145del , LRG_680t1:c.114+141_114+145del	NP_998839.1:n.114+141_114+145del
XR_929320.1:n.222+141_222+145del
XR_929321.1:n.222+141_222+145del
XR_929322.1:n.222+141_222+145del
XR_929323.1:n.222+141_222+145del
XR_929324.1:n.225+141_225+145del
XR_929325.1:n.222+141_222+145del
XM_017015087.2:c.114+141_114+145del	XP_016870576.1:n.114+141_114+145del
XM_017015088.2:c.114+141_114+145del	XP_016870577.1:n.114+141_114+145del
XM_017015090.2:c.114+141_114+145del	XP_016870579.1:n.114+141_114+145del
XM_017015091.2:c.114+141_114+145del	XP_016870580.1:n.114+141_114+145del
XM_017015092.2:c.114+141_114+145del	XP_016870581.1:n.114+141_114+145del
XM_017015093.2:c.114+141_114+145del	XP_016870582.1:n.114+141_114+145del
NM_001301226.2:c.114+141_114+145del	NP_001288155.1:n.114+141_114+145del
NM_003289.4:c.114+141_114+145del MANE Select	NP_003280.2:n.114+141_114+145del
NM_001301227.2:c.114+141_114+145del	NP_001288156.1:n.114+141_114+145del