Canonical Allele Identifier: CA2810629104

Gene: ACTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511283_81511284insAG , CM000679.2:g.81511283_81511284insAG	GRCh38
NC_000017.10:g.79478309_79478310insAG , CM000679.1:g.79478309_79478310insAG	GRCh37
NC_000017.9:g.77092904_77092905insAG	NCBI36
NG_011433.1:g.6518_6519insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.706_707insCT	ENSP00000466346.2:p.Leu236ProfsTer?
ENST00000571691.6:c.634_635insCT	ENSP00000461407.2:p.Leu212ProfsTer?
ENST00000571721.6:c.706_707insCT	ENSP00000460660.2:p.Leu236ProfsTer?
ENST00000572105.7:c.*150_*151insCT	ENSP00000462823.1:n.*150_*151insCT
ENST00000573283.7:c.706_707insCT MANE Select	ENSP00000458435.1:p.Leu236ProfsTer?
ENST00000574671.6:n.1106_1107insCT
ENST00000575659.6:c.706_707insCT	ENSP00000459119.2:p.Leu236ProfsTer?
ENST00000575994.6:c.706_707insCT	ENSP00000460464.2:p.Leu236ProfsTer?
ENST00000576214.3:n.1007_1008insCT
ENST00000576544.6:c.706_707insCT	ENSP00000461672.1:p.Leu236ProfsTer?
ENST00000615544.5:c.706_707insCT	ENSP00000477968.1:p.Leu236ProfsTer?
ENST00000644774.2:c.679_680insCT	ENSP00000493648.2:p.Leu227ProfsTer?
ENST00000679410.1:n.830_831insCT
ENST00000679480.1:c.706_707insCT	ENSP00000506201.1:p.Leu236ProfsTer?
ENST00000679535.1:n.1007_1008insCT
ENST00000679778.1:c.706_707insCT	ENSP00000505235.1:p.Leu236ProfsTer?
ENST00000680227.1:c.706_707insCT	ENSP00000506253.1:p.Leu236ProfsTer?
ENST00000680727.1:c.706_707insCT	ENSP00000505193.1:p.Leu236ProfsTer?
ENST00000681052.1:c.706_707insCT	ENSP00000505060.1:p.Leu236ProfsTer?
ENST00000681092.1:c.*510_*511insCT	ENSP00000506720.1:n.*510_*511insCT
ENST00000681842.1:c.706_707insCT	ENSP00000506126.1:p.Leu236ProfsTer?
ENST00000331925.6:c.706_707insCT	ENSP00000331514.2:p.Leu236ProfsTer?
ENST00000571691.5:c.679_680insCT	ENSP00000461407.1:p.Leu227ProfsTer?
ENST00000572105.6:c.*150_*151insCT	ENSP00000462823.1:n.*150_*151insCT
ENST00000573283.5:c.706_707insCT	ENSP00000458435.1:p.Leu236ProfsTer?
ENST00000574671.5:n.565_566insCT
ENST00000575087.5:c.706_707insCT	ENSP00000459124.1:p.Leu236ProfsTer?
ENST00000575842.5:c.706_707insCT	ENSP00000458162.1:p.Leu236ProfsTer?
ENST00000576209.5:n.591_592insCT
ENST00000576214.2:n.904_905insCT
ENST00000576544.5:c.706_707insCT	ENSP00000461672.1:p.Leu236ProfsTer?
ENST00000576917.5:n.759_760insCT
ENST00000615544.4:c.706_707insCT	ENSP00000477968.1:p.Leu236ProfsTer?
NM_001199954.1:c.706_707insCT	NP_001186883.1:p.Leu236ProfsTer?
NM_001614.3:c.706_707insCT	NP_001605.1:p.Leu236ProfsTer?
NR_037688.1:n.845_846insCT
NM_001199954.2:c.706_707insCT	NP_001186883.1:p.Leu236ProfsTer?
NM_001614.4:c.706_707insCT	NP_001605.1:p.Leu236ProfsTer?
NR_037688.2:n.778_779insCT
NM_001614.5:c.706_707insCT MANE Select	NP_001605.1:p.Leu236ProfsTer?
NR_037688.3:n.778_779insCT
NM_001199954.3:c.706_707insCT	NP_001186883.1:p.Leu236ProfsTer?