Canonical Allele Identifier: CA2144501730
Gene: ACTN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68874140T= , CM000676.2:g.68874140T= GRCh38
NC_000014.8:g.69340857T= , CM000676.1:g.69340857T= GRCh37
NC_000014.7:g.68410610T= NCBI36
NG_029480.1:g.110227A= , LRG_886:g.110227A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553882.2:n.2896A=
ENST00000682130.1:n.4705A=
ENST00000682291.1:c.*719A= ENSP00000507093.1:n.*719A=
ENST00000682298.1:n.5054A=
ENST00000682331.1:c.*719A= ENSP00000508329.1:n.*719A=
ENST00000682378.1:n.5434A=
ENST00000682381.1:n.4969A=
ENST00000682522.1:n.3353A=
ENST00000683069.1:n.4800A=
ENST00000683198.1:c.*719A= ENSP00000507889.1:n.*719A=
ENST00000683225.1:c.*719A= ENSP00000506977.1:n.*719A=
ENST00000683267.1:c.*2676A= ENSP00000508356.1:n.*2676A=
ENST00000683780.1:n.4310A=
ENST00000684146.1:n.4217A=
ENST00000684182.1:c.*719A= ENSP00000508177.1:n.*719A=
ENST00000684287.1:n.2730A=
ENST00000684340.1:n.4888A=
ENST00000684598.1:c.*719A= ENSP00000507785.1:n.*719A=
ENST00000684638.1:c.*2742A= ENSP00000507609.1:n.*2742A=
ENST00000684639.1:c.*719A= ENSP00000507653.1:n.*719A=
ENST00000394419.9:c.*719A= MANE Select ENSP00000377941.4:n.*719A=
NM_001102.3:c.*719A= NP_001093.1:n.*719A=
NM_001130004.1:c.*719A= , LRG_886t1:c.*719A= NP_001123476.1:n.*719A=
NM_001130005.1:c.*719A= NP_001123477.1:n.*719A=
XM_011537265.1:c.*719A= XP_011535567.1:n.*719A=
XM_011537266.1:c.*719A= XP_011535568.1:n.*719A=
XM_011537267.1:c.*719A= XP_011535569.1:n.*719A=
XM_011537268.1:c.*719A= XP_011535570.1:n.*719A=
XM_011537269.1:c.*719A= XP_011535571.1:n.*719A=
XM_011537270.1:c.*719A= XP_011535572.1:n.*719A=
XM_011537271.1:c.*719A= XP_011535573.1:n.*719A=
XM_011537265.2:c.*719A= XP_011535567.1:n.*719A=
XM_011537266.3:c.*719A= XP_011535568.1:n.*719A=
XM_011537267.3:c.*719A= XP_011535569.1:n.*719A=
XM_011537268.3:c.*719A= XP_011535570.1:n.*719A=
XM_017021720.1:c.*719A= XP_016877209.1:n.*719A=
XM_017021722.2:c.*719A= XP_016877211.1:n.*719A=
XM_017021725.1:c.*719A= XP_016877214.1:n.*719A=
XM_017021727.2:c.*719A= XP_016877216.1:n.*719A=
XM_017021728.2:c.*719A= XP_016877217.1:n.*719A=
NM_001102.4:c.*719A= NP_001093.1:n.*719A=
NM_001130005.2:c.*719A= NP_001123477.1:n.*719A=
NM_001130004.2:c.*719A= MANE Select NP_001123476.1:n.*719A=