Canonical Allele Identifier: CA919908508

Gene: ACTG1

Linked Data

• dbSNP Id: rs1598548003

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511181_81511191del , CM000679.2:g.81511181_81511191del	GRCh38
NC_000017.10:g.79478207_79478217del , CM000679.1:g.79478207_79478217del	GRCh37
NC_000017.9:g.77092802_77092812del	NCBI36
NG_011433.1:g.6611_6621del

Transcript Alleles

HGVS	Amino-acid change
ENST00000570382.2:c.799_802+7del
ENST00000571691.6:c.727_730+7del
ENST00000571721.6:c.799_802+7del
ENST00000572105.7:c.*243_*246+7del
ENST00000573283.7:c.799_802+7del
ENST00000574671.6:n.1199_1202+7del
ENST00000575659.6:c.799_802+7del
ENST00000575994.6:c.799_802+7del
ENST00000576214.3:n.1100_1103+7del
ENST00000576544.6:c.799_802+7del
ENST00000615544.5:c.799_802+7del
ENST00000644774.2:c.772_775+7del
ENST00000679410.1:n.923_933del
ENST00000679480.1:c.799_802+7del
ENST00000679535.1:n.1100_1103+7del
ENST00000679778.1:c.799_802+7del
ENST00000680227.1:c.799_802+7del
ENST00000680727.1:c.799_802+7del
ENST00000681052.1:c.799_802+7del
ENST00000681092.1:c.*603_*606+7del
ENST00000681842.1:c.799_802+7del
ENST00000331925.6:c.799_802+7del
ENST00000572105.6:c.*243_*246+7del
ENST00000573283.5:c.799_802+7del
ENST00000574671.5:n.658_661+7del
ENST00000575087.5:c.799_802+7del
ENST00000575842.5:c.799_802+7del
ENST00000576209.5:n.684_687+7del
ENST00000576214.2:n.997_1000+7del
ENST00000576544.5:c.799_802+7del
ENST00000576917.5:n.852_862del
ENST00000615544.4:c.799_802+7del
NM_001199954.1:c.799_802+7del
NM_001614.3:c.799_802+7del
NR_037688.1:n.938_941+7del
NM_001199954.2:c.799_802+7del
NM_001614.4:c.799_802+7del
NR_037688.2:n.871_874+7del
NM_001614.5:c.799_802+7del
NR_037688.3:n.871_874+7del
NM_001199954.3:c.799_802+7del