Canonical Allele Identifier: CA8836233

Gene: ACTG1

Linked Data

• dbSNP Id: rs782049770
• ExAC: 17:79478871 C / CAT
• gnomAD v2: 17-79478871-C-CAT
• gnomAD v3: 17-81511845-C-CAT
• gnomAD v4: 17-81511845-C-CAT
• MyVariant Identifiers: chr17:g.79478871_79478872insAT (hg19) ; chr17:g.81511845_81511846insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511845_81511846insAT , CM000679.2:g.81511845_81511846insAT	GRCh38
NC_000017.10:g.79478871_79478872insAT , CM000679.1:g.79478871_79478872insAT	GRCh37
NC_000017.9:g.77093466_77093467insAT	NCBI36
NG_011433.1:g.5956_5957insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.363+57_363+58insAT	ENSP00000466346.2:n.363+57_363+58insAT
ENST00000571691.6:c.339+81_339+82insAT	ENSP00000461407.2:n.339+81_339+82insAT
ENST00000571721.6:c.363+57_363+58insAT	ENSP00000460660.2:n.363+57_363+58insAT
ENST00000572105.7:c.364-43_364-42insAT	ENSP00000462823.1:n.364-43_364-42insAT
ENST00000573283.7:c.363+57_363+58insAT MANE Select	ENSP00000458435.1:n.363+57_363+58insAT
ENST00000574671.6:n.544_545insAT
ENST00000575659.6:c.363+57_363+58insAT	ENSP00000459119.2:n.363+57_363+58insAT
ENST00000575994.6:c.363+57_363+58insAT	ENSP00000460464.2:n.363+57_363+58insAT
ENST00000576214.3:n.488-43_488-42insAT
ENST00000576544.6:c.363+57_363+58insAT	ENSP00000461672.1:n.363+57_363+58insAT
ENST00000615544.5:c.363+57_363+58insAT	ENSP00000477968.1:n.363+57_363+58insAT
ENST00000644774.2:c.336+57_336+58insAT	ENSP00000493648.2:n.336+57_336+58insAT
ENST00000679410.1:n.487+57_487+58insAT
ENST00000679480.1:c.363+57_363+58insAT	ENSP00000506201.1:n.363+57_363+58insAT
ENST00000679535.1:n.488-43_488-42insAT
ENST00000679778.1:c.363+57_363+58insAT	ENSP00000505235.1:n.363+57_363+58insAT
ENST00000680227.1:c.363+57_363+58insAT	ENSP00000506253.1:n.363+57_363+58insAT
ENST00000680727.1:c.363+57_363+58insAT	ENSP00000505193.1:n.363+57_363+58insAT
ENST00000681052.1:c.363+57_363+58insAT	ENSP00000505060.1:n.363+57_363+58insAT
ENST00000681092.1:c.*167+57_*167+58insAT	ENSP00000506720.1:n.*167+57_*167+58insAT
ENST00000681842.1:c.363+57_363+58insAT	ENSP00000506126.1:n.363+57_363+58insAT
ENST00000331925.6:c.363+57_363+58insAT	ENSP00000331514.2:n.363+57_363+58insAT
ENST00000570382.1:c.339+81_339+82insAT	ENSP00000466346.1:n.339+81_339+82insAT
ENST00000571691.5:c.336+57_336+58insAT	ENSP00000461407.1:n.336+57_336+58insAT
ENST00000571721.5:c.363+57_363+58insAT	ENSP00000460660.1:n.363+57_363+58insAT
ENST00000572105.6:c.364-43_364-42insAT	ENSP00000462823.1:n.364-43_364-42insAT
ENST00000573283.5:c.363+57_363+58insAT	ENSP00000458435.1:n.363+57_363+58insAT
ENST00000574671.5:n.3_4insAT
ENST00000575087.5:c.363+57_363+58insAT	ENSP00000459124.1:n.363+57_363+58insAT
ENST00000575659.5:c.363+57_363+58insAT	ENSP00000459119.1:n.363+57_363+58insAT
ENST00000575842.5:c.363+57_363+58insAT	ENSP00000458162.1:n.363+57_363+58insAT
ENST00000575994.5:c.363+57_363+58insAT	ENSP00000460464.1:n.363+57_363+58insAT
ENST00000576209.5:n.248+57_248+58insAT
ENST00000576214.2:n.385-43_385-42insAT
ENST00000576544.5:c.363+57_363+58insAT	ENSP00000461672.1:n.363+57_363+58insAT
ENST00000576917.5:n.416+57_416+58insAT
ENST00000615544.4:c.363+57_363+58insAT	ENSP00000477968.1:n.363+57_363+58insAT
NM_001199954.1:c.363+57_363+58insAT	NP_001186883.1:n.363+57_363+58insAT
NM_001614.3:c.363+57_363+58insAT	NP_001605.1:n.363+57_363+58insAT
NR_037688.1:n.502+57_502+58insAT
NM_001199954.2:c.363+57_363+58insAT	NP_001186883.1:n.363+57_363+58insAT
NM_001614.4:c.363+57_363+58insAT	NP_001605.1:n.363+57_363+58insAT
NR_037688.2:n.435+57_435+58insAT
NM_001614.5:c.363+57_363+58insAT MANE Select	NP_001605.1:n.363+57_363+58insAT
NR_037688.3:n.435+57_435+58insAT
NM_001199954.3:c.363+57_363+58insAT	NP_001186883.1:n.363+57_363+58insAT