Canonical Allele Identifier: CA2144552305
Gene: ACTN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68978886A= , CM000676.2:g.68978886A= GRCh38
NC_000014.8:g.69445603A= , CM000676.1:g.69445603A= GRCh37
NC_000014.7:g.68515356A= NCBI36
NG_029480.1:g.5481T= , LRG_886:g.5481T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682130.1:n.393+66T=
ENST00000682291.1:c.105+66T= ENSP00000507093.1:n.105+66T=
ENST00000682298.1:n.393+66T=
ENST00000682331.1:c.105+66T= ENSP00000508329.1:n.105+66T=
ENST00000682378.1:n.393+66T=
ENST00000682381.1:n.393+66T=
ENST00000682559.1:c.105+66T= ENSP00000507271.1:n.105+66T=
ENST00000682602.1:n.199+66T=
ENST00000683069.1:n.393+66T=
ENST00000683198.1:c.105+66T= ENSP00000507889.1:n.105+66T=
ENST00000683261.1:n.393+66T=
ENST00000683267.1:c.105+66T= ENSP00000508356.1:n.105+66T=
ENST00000683342.1:c.105+66T= ENSP00000508301.1:n.105+66T=
ENST00000683780.1:n.393+66T=
ENST00000684146.1:n.393+66T=
ENST00000684340.1:n.393+66T=
ENST00000684598.1:c.105+66T= ENSP00000507785.1:n.105+66T=
ENST00000684638.1:c.105+66T= ENSP00000507609.1:n.105+66T=
ENST00000684639.1:c.105+66T= ENSP00000507653.1:n.105+66T=
ENST00000684713.1:c.105+66T= ENSP00000507155.1:n.105+66T=
ENST00000394419.9:c.105+66T= MANE Select ENSP00000377941.4:n.105+66T=
ENST00000679147.1:c.105+66T= ENSP00000504355.1:n.105+66T=
ENST00000193403.10:c.105+66T= ENSP00000193403.6:n.105+66T=
ENST00000394419.8:c.105+66T= ENSP00000377941.4:n.105+66T=
ENST00000438964.6:c.105+66T= ENSP00000414272.2:n.105+66T=
ENST00000538545.6:c.105+66T= ENSP00000439828.2:n.105+66T=
ENST00000556203.1:n.80+66T=
NM_001102.3:c.105+66T= NP_001093.1:n.105+66T=
NM_001130004.1:c.105+66T= , LRG_886t1:c.105+66T= NP_001123476.1:n.105+66T=
NM_001130005.1:c.105+66T= NP_001123477.1:n.105+66T=
XM_011537269.1:c.105+66T= XP_011535571.1:n.105+66T=
XM_017021722.2:c.105+66T= XP_016877211.1:n.105+66T=
XM_017021723.2:c.105+66T= XP_016877212.1:n.105+66T=
XM_017021727.2:c.105+66T= XP_016877216.1:n.105+66T=
NM_001102.4:c.105+66T= NP_001093.1:n.105+66T=
NM_001130005.2:c.105+66T= NP_001123477.1:n.105+66T=
NM_001130004.2:c.105+66T= MANE Select NP_001123476.1:n.105+66T=