Canonical Allele Identifier: CA986848628
Gene: ACTG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81511161_81511198del , CM000679.2:g.81511161_81511198del GRCh38
NC_000017.10:g.79478187_79478224del , CM000679.1:g.79478187_79478224del GRCh37
NC_000017.9:g.77092782_77092819del NCBI36
NG_011433.1:g.6604_6641del

Transcript Alleles

HGVS Amino-acid change
ENST00000570382.2:c.792_802+27del
ENST00000571691.6:c.720_730+27del
ENST00000571721.6:c.792_802+27del
ENST00000572105.7:c.*236_*246+27del
ENST00000573283.7:c.792_802+27del
ENST00000574671.6:n.1192_1202+27del
ENST00000575659.6:c.792_802+27del
ENST00000575994.6:c.792_802+27del
ENST00000576214.3:n.1093_1103+27del
ENST00000576544.6:c.792_802+27del
ENST00000615544.5:c.792_802+27del
ENST00000644774.2:c.765_775+27del
ENST00000679410.1:n.916_953del
ENST00000679480.1:c.792_802+27del
ENST00000679535.1:n.1093_1103+27del
ENST00000679778.1:c.792_802+27del
ENST00000680227.1:c.792_802+27del
ENST00000680727.1:c.792_802+27del
ENST00000681052.1:c.792_802+27del
ENST00000681092.1:c.*596_*606+27del
ENST00000681842.1:c.792_802+27del
ENST00000331925.6:c.792_802+27del
ENST00000572105.6:c.*236_*246+27del
ENST00000573283.5:c.792_802+27del
ENST00000574671.5:n.651_661+27del
ENST00000575087.5:c.792_802+27del
ENST00000575842.5:c.792_802+27del
ENST00000576209.5:n.677_687+27del
ENST00000576214.2:n.990_1000+27del
ENST00000576544.5:c.792_802+27del
ENST00000576917.5:n.845_882del
ENST00000615544.4:c.792_802+27del
NM_001199954.1:c.792_802+27del
NM_001614.3:c.792_802+27del
NR_037688.1:n.931_941+27del
NM_001199954.2:c.792_802+27del
NM_001614.4:c.792_802+27del
NR_037688.2:n.864_874+27del
NM_001614.5:c.792_802+27del
NR_037688.3:n.864_874+27del
NM_001199954.3:c.792_802+27del