Canonical Allele Identifier: CA16608694

Gene: ACTG1

Linked Data

• ClinVar Variation Id: 384952
• ClinVar RCV Id: RCV000441592
• dbSNP Id: rs1057522087
• gnomAD v2: 17-79479796-A-T
• gnomAD v3: 17-81512770-A-T
• gnomAD v4: 17-81512770-A-T
• MyVariant Identifiers: chr17:g.79479796A>T (hg19) ; chr17:g.81512770A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512770A>T , CM000679.2:g.81512770A>T	GRCh38
NC_000017.10:g.79479796A>T , CM000679.1:g.79479796A>T	GRCh37
NC_000017.9:g.77094391A>T	NCBI36
NG_011433.1:g.5032T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-162T>A	ENSP00000466346.2:n.-162T>A
ENST00000571691.6:c.-43T>A	ENSP00000461407.2:n.-43T>A
ENST00000571721.6:c.-313T>A	ENSP00000460660.2:n.-313T>A
ENST00000572105.7:c.-43T>A	ENSP00000462823.1:n.-43T>A
ENST00000573283.7:c.-43T>A MANE Select	ENSP00000458435.1:n.-43T>A
ENST00000574671.6:n.82T>A
ENST00000575659.6:c.-6-410T>A	ENSP00000459119.2:n.-6-410T>A
ENST00000575994.6:c.-6-410T>A	ENSP00000460464.2:n.-6-410T>A
ENST00000576214.3:n.82T>A
ENST00000576544.6:c.-43T>A	ENSP00000461672.1:n.-43T>A
ENST00000615544.5:c.-6-410T>A	ENSP00000477968.1:n.-6-410T>A
ENST00000679410.1:n.82T>A
ENST00000679535.1:n.82T>A
ENST00000679778.1:c.-6-410T>A	ENSP00000505235.1:n.-6-410T>A
ENST00000680227.1:c.-162T>A	ENSP00000506253.1:n.-162T>A
ENST00000681052.1:c.-43T>A	ENSP00000505060.1:n.-43T>A
ENST00000681092.1:c.-43T>A	ENSP00000506720.1:n.-43T>A
ENST00000681842.1:c.-43T>A	ENSP00000506126.1:n.-43T>A
ENST00000331925.6:c.-43T>A	ENSP00000331514.2:n.-43T>A
ENST00000570382.1:c.-43T>A	ENSP00000466346.1:n.-43T>A
ENST00000571721.5:c.-313T>A	ENSP00000460660.1:n.-313T>A
ENST00000572105.6:c.-43T>A	ENSP00000462823.1:n.-43T>A
ENST00000573283.5:c.-162T>A	ENSP00000458435.1:n.-162T>A
ENST00000575087.5:c.-171T>A	ENSP00000459124.1:n.-171T>A
ENST00000575659.5:c.-6-410T>A	ENSP00000459119.1:n.-6-410T>A
ENST00000575842.5:c.-416T>A	ENSP00000458162.1:n.-416T>A
ENST00000575994.5:c.-6-410T>A	ENSP00000460464.1:n.-6-410T>A
ENST00000576544.5:c.-43T>A	ENSP00000461672.1:n.-43T>A
ENST00000576917.5:n.11T>A
NM_001199954.1:c.-162T>A	NP_001186883.1:n.-162T>A
NM_001614.3:c.-43T>A	NP_001605.1:n.-43T>A
NR_037688.1:n.97T>A
NM_001199954.2:c.-162T>A	NP_001186883.1:n.-162T>A
NM_001614.4:c.-43T>A	NP_001605.1:n.-43T>A
NR_037688.2:n.30T>A
NM_001614.5:c.-43T>A MANE Select	NP_001605.1:n.-43T>A
NR_037688.3:n.30T>A
NM_001199954.3:c.-162T>A	NP_001186883.1:n.-162T>A