Canonical Allele Identifier: CA628022594

Gene: ACTG1

Linked Data

• dbSNP Id: rs1555666935
• gnomAD v2: 17-79478831-TG-T
• gnomAD v4: 17-81511805-TG-T
• MyVariant Identifiers: chr17:g.79478832del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511807del , CM000679.2:g.81511807del	GRCh38
NC_000017.10:g.79478833del , CM000679.1:g.79478833del	GRCh37
NC_000017.9:g.77093428del	NCBI36
NG_011433.1:g.5996del

Transcript Alleles

HGVS	Amino-acid change
ENST00000570382.2:c.363+97del	ENSP00000466346.2:n.363+97del
ENST00000571691.6:c.339+121del	ENSP00000461407.2:n.339+121del
ENST00000571721.6:c.363+97del	ENSP00000460660.2:n.363+97del
ENST00000572105.7:c.364-3del	ENSP00000462823.1:n.364-3del
ENST00000573283.7:c.363+97del MANE Select	ENSP00000458435.1:n.363+97del
ENST00000574671.6:n.584del
ENST00000575659.6:c.363+97del	ENSP00000459119.2:n.363+97del
ENST00000575994.6:c.363+97del	ENSP00000460464.2:n.363+97del
ENST00000576214.3:n.488-3del
ENST00000576544.6:c.363+97del	ENSP00000461672.1:n.363+97del
ENST00000615544.5:c.363+97del	ENSP00000477968.1:n.363+97del
ENST00000644774.2:c.336+97del	ENSP00000493648.2:n.336+97del
ENST00000679410.1:n.487+97del
ENST00000679480.1:c.363+97del	ENSP00000506201.1:n.363+97del
ENST00000679535.1:n.488-3del
ENST00000679778.1:c.363+97del	ENSP00000505235.1:n.363+97del
ENST00000680227.1:c.363+97del	ENSP00000506253.1:n.363+97del
ENST00000680727.1:c.363+97del	ENSP00000505193.1:n.363+97del
ENST00000681052.1:c.363+97del	ENSP00000505060.1:n.363+97del
ENST00000681092.1:c.*167+97del	ENSP00000506720.1:n.*167+97del
ENST00000681842.1:c.363+97del	ENSP00000506126.1:n.363+97del
ENST00000331925.6:c.363+97del	ENSP00000331514.2:n.363+97del
ENST00000570382.1:c.339+121del	ENSP00000466346.1:n.339+121del
ENST00000571691.5:c.336+97del	ENSP00000461407.1:n.336+97del
ENST00000571721.5:c.363+97del	ENSP00000460660.1:n.363+97del
ENST00000572105.6:c.364-3del	ENSP00000462823.1:n.364-3del
ENST00000573283.5:c.363+97del	ENSP00000458435.1:n.363+97del
ENST00000574671.5:n.43del
ENST00000575087.5:c.363+97del	ENSP00000459124.1:n.363+97del
ENST00000575659.5:c.363+97del	ENSP00000459119.1:n.363+97del
ENST00000575842.5:c.363+97del	ENSP00000458162.1:n.363+97del
ENST00000575994.5:c.363+97del	ENSP00000460464.1:n.363+97del
ENST00000576209.5:n.248+97del
ENST00000576214.2:n.385-3del
ENST00000576544.5:c.363+97del	ENSP00000461672.1:n.363+97del
ENST00000576917.5:n.416+97del
ENST00000615544.4:c.363+97del	ENSP00000477968.1:n.363+97del
NM_001199954.1:c.363+97del	NP_001186883.1:n.363+97del
NM_001614.3:c.363+97del	NP_001605.1:n.363+97del
NR_037688.1:n.502+97del
NM_001199954.2:c.363+97del	NP_001186883.1:n.363+97del
NM_001614.4:c.363+97del	NP_001605.1:n.363+97del
NR_037688.2:n.435+97del
NM_001614.5:c.363+97del MANE Select	NP_001605.1:n.363+97del
NR_037688.3:n.435+97del
NM_001199954.3:c.363+97del	NP_001186883.1:n.363+97del