Canonical Allele Identifier: CA7242245

Gene: ACTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68882485G>A , CM000676.2:g.68882485G>A	GRCh38
NC_000014.8:g.69349202G>A , CM000676.1:g.69349202G>A	GRCh37
NC_000014.7:g.68418955G>A	NCBI36
NG_029480.1:g.101882C>T , LRG_886:g.101882C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682130.1:n.2031C>T
ENST00000682291.1:c.1926C>T	ENSP00000507093.1:p.Ile642=
ENST00000682298.1:n.2299C>T
ENST00000682331.1:c.1743C>T	ENSP00000508329.1:p.Ile581=
ENST00000682378.1:n.2214C>T
ENST00000682381.1:n.2214C>T
ENST00000682522.1:n.1815C>T
ENST00000682559.1:c.*1379C>T	ENSP00000507271.1:n.*1379C>T
ENST00000683069.1:n.2126C>T
ENST00000683198.1:c.1950C>T	ENSP00000507889.1:p.Ile650=
ENST00000683225.1:c.1731C>T	ENSP00000506977.1:p.Ile577=
ENST00000683267.1:c.*1204C>T	ENSP00000508356.1:n.*1204C>T
ENST00000683342.1:c.1926C>T	ENSP00000508301.1:p.Ile642=
ENST00000683780.1:n.2772C>T
ENST00000684146.1:n.2214C>T
ENST00000684182.1:c.1731C>T	ENSP00000508177.1:p.Ile577=
ENST00000684287.1:n.1192C>T
ENST00000684340.1:n.2214C>T
ENST00000684598.1:c.1926C>T	ENSP00000507785.1:p.Ile642=
ENST00000684638.1:c.*1204C>T	ENSP00000507609.1:n.*1204C>T
ENST00000684639.1:c.1806C>T	ENSP00000507653.1:p.Ile602=
ENST00000684713.1:c.1833C>T	ENSP00000507155.1:p.Ile611=
ENST00000394419.9:c.1926C>T MANE Select	ENSP00000377941.4:p.Ile642=
ENST00000679147.1:c.1950C>T	ENSP00000504355.1:p.Ile650=
ENST00000193403.10:c.1926C>T	ENSP00000193403.6:p.Ile642=
ENST00000376839.7:c.1731C>T	ENSP00000366035.3:p.Ile577=
ENST00000394419.8:c.1926C>T	ENSP00000377941.4:p.Ile642=
ENST00000438964.6:c.1926C>T	ENSP00000414272.2:p.Ile642=
ENST00000538545.6:c.1926C>T	ENSP00000439828.2:p.Ile642=
ENST00000544964.6:c.588+388C>T	ENSP00000444422.2:n.588+388C>T
ENST00000553290.1:c.244C>T
ENST00000555075.5:c.83C>T
ENST00000556083.1:n.3380C>T
NM_001102.3:c.1926C>T	NP_001093.1:p.Ile642=
NM_001130004.1:c.1926C>T , LRG_886t1:c.1926C>T	NP_001123476.1:p.Ile642=
NM_001130005.1:c.1926C>T	NP_001123477.1:p.Ile642=
XM_011537265.1:c.2037C>T	XP_011535567.1:p.Ile679=
XM_011537266.1:c.2037C>T	XP_011535568.1:p.Ile679=
XM_011537267.1:c.2013C>T	XP_011535569.1:p.Ile671=
XM_011537268.1:c.2013C>T	XP_011535570.1:p.Ile671=
XM_011537269.1:c.1950C>T	XP_011535571.1:p.Ile650=
XM_011537270.1:c.1887C>T	XP_011535572.1:p.Ile629=
XM_011537271.1:c.1863C>T	XP_011535573.1:p.Ile621=
XM_011537265.2:c.2037C>T	XP_011535567.1:p.Ile679=
XM_011537266.3:c.2037C>T	XP_011535568.1:p.Ile679=
XM_011537267.3:c.2013C>T	XP_011535569.1:p.Ile671=
XM_011537268.3:c.2013C>T	XP_011535570.1:p.Ile671=
XM_017021720.1:c.2037C>T	XP_016877209.1:p.Ile679=
XM_017021721.2:c.2013C>T	XP_016877210.1:p.Ile671=
XM_017021722.2:c.1950C>T	XP_016877211.1:p.Ile650=
XM_017021723.2:c.1926C>T	XP_016877212.1:p.Ile642=
XM_017021725.1:c.1887C>T	XP_016877214.1:p.Ile629=
XM_017021726.2:c.1863C>T	XP_016877215.1:p.Ile621=
XM_017021727.2:c.1950C>T	XP_016877216.1:p.Ile650=
XM_017021728.2:c.1863C>T	XP_016877217.1:p.Ile621=
NM_001102.4:c.1926C>T	NP_001093.1:p.Ile642=
NM_001130005.2:c.1926C>T	NP_001123477.1:p.Ile642=
NM_001130004.2:c.1926C>T MANE Select	NP_001123476.1:p.Ile642=