Canonical Allele Identifier: CA2278540997

Gene: ACTG1

Linked Data

• dbSNP Id: rs2031905483

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512774_81512776del , CM000679.2:g.81512774_81512776del	GRCh38
NC_000017.10:g.79479800_79479802del , CM000679.1:g.79479800_79479802del	GRCh37
NC_000017.9:g.77094395_77094397del	NCBI36
NG_011433.1:g.5026_5028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-168_-166del	ENSP00000466346.2:n.-168_-166del
ENST00000571691.6:c.-49_-47del	ENSP00000461407.2:n.-49_-47del
ENST00000571721.6:c.-319_-317del	ENSP00000460660.2:n.-319_-317del
ENST00000572105.7:c.-49_-47del	ENSP00000462823.1:n.-49_-47del
ENST00000573283.7:c.-49_-47del MANE Select	ENSP00000458435.1:n.-49_-47del
ENST00000574671.6:n.76_78del
ENST00000575659.6:c.-6-416_-6-414del	ENSP00000459119.2:n.-6-416_-6-414del
ENST00000575994.6:c.-6-416_-6-414del	ENSP00000460464.2:n.-6-416_-6-414del
ENST00000576214.3:n.76_78del
ENST00000576544.6:c.-49_-47del	ENSP00000461672.1:n.-49_-47del
ENST00000615544.5:c.-6-416_-6-414del	ENSP00000477968.1:n.-6-416_-6-414del
ENST00000679410.1:n.76_78del
ENST00000679535.1:n.76_78del
ENST00000679778.1:c.-6-416_-6-414del	ENSP00000505235.1:n.-6-416_-6-414del
ENST00000680227.1:c.-168_-166del	ENSP00000506253.1:n.-168_-166del
ENST00000681052.1:c.-49_-47del	ENSP00000505060.1:n.-49_-47del
ENST00000681092.1:c.-49_-47del	ENSP00000506720.1:n.-49_-47del
ENST00000681842.1:c.-49_-47del	ENSP00000506126.1:n.-49_-47del
ENST00000331925.6:c.-49_-47del	ENSP00000331514.2:n.-49_-47del
ENST00000570382.1:c.-49_-47del	ENSP00000466346.1:n.-49_-47del
ENST00000571721.5:c.-319_-317del	ENSP00000460660.1:n.-319_-317del
ENST00000572105.6:c.-49_-47del	ENSP00000462823.1:n.-49_-47del
ENST00000573283.5:c.-168_-166del	ENSP00000458435.1:n.-168_-166del
ENST00000575087.5:c.-177_-175del	ENSP00000459124.1:n.-177_-175del
ENST00000575659.5:c.-6-416_-6-414del	ENSP00000459119.1:n.-6-416_-6-414del
ENST00000575842.5:c.-422_-420del	ENSP00000458162.1:n.-422_-420del
ENST00000575994.5:c.-6-416_-6-414del	ENSP00000460464.1:n.-6-416_-6-414del
ENST00000576544.5:c.-49_-47del	ENSP00000461672.1:n.-49_-47del
ENST00000576917.5:n.5_7del
NM_001199954.1:c.-168_-166del	NP_001186883.1:n.-168_-166del
NM_001614.3:c.-49_-47del	NP_001605.1:n.-49_-47del
NR_037688.1:n.91_93del
NM_001199954.2:c.-168_-166del	NP_001186883.1:n.-168_-166del
NM_001614.4:c.-49_-47del	NP_001605.1:n.-49_-47del
NR_037688.2:n.24_26del
NM_001614.5:c.-49_-47del MANE Select	NP_001605.1:n.-49_-47del
NR_037688.3:n.24_26del
NM_001199954.3:c.-168_-166del	NP_001186883.1:n.-168_-166del