Canonical Allele Identifier: CA390190984

Gene: ACTN1

Linked Data

• MyVariant Identifiers: chr14:g.69371393G>T (hg19) ; chr14:g.68904676G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68904676G>T , CM000676.2:g.68904676G>T	GRCh38
NC_000014.8:g.69371393G>T , CM000676.1:g.69371393G>T	GRCh37
NC_000014.7:g.68441146G>T	NCBI36
NG_029480.1:g.79691C>A , LRG_886:g.79691C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000554508.6:c.460C>A	ENSP00000507578.1:p.Pro154Thr
ENST00000682130.1:n.943C>A
ENST00000682291.1:c.655C>A	ENSP00000507093.1:p.Pro219Thr
ENST00000682298.1:n.943C>A
ENST00000682331.1:c.655C>A	ENSP00000508329.1:p.Pro219Thr
ENST00000682378.1:n.943C>A
ENST00000682381.1:n.943C>A
ENST00000682522.1:n.544C>A
ENST00000682559.1:c.*108C>A	ENSP00000507271.1:n.*108C>A
ENST00000683069.1:n.855C>A
ENST00000683198.1:c.655C>A	ENSP00000507889.1:p.Pro219Thr
ENST00000683225.1:c.460C>A	ENSP00000506977.1:p.Pro154Thr
ENST00000683261.1:n.943C>A
ENST00000683267.1:c.655C>A	ENSP00000508356.1:p.Pro219Thr
ENST00000683342.1:c.655C>A	ENSP00000508301.1:p.Pro219Thr
ENST00000683780.1:n.1501C>A
ENST00000684096.1:n.1114C>A
ENST00000684146.1:n.943C>A
ENST00000684182.1:c.460C>A	ENSP00000508177.1:p.Pro154Thr
ENST00000684340.1:n.943C>A
ENST00000684598.1:c.655C>A	ENSP00000507785.1:p.Pro219Thr
ENST00000684638.1:c.655C>A	ENSP00000507609.1:p.Pro219Thr
ENST00000684639.1:c.535C>A	ENSP00000507653.1:p.Pro179Thr
ENST00000684713.1:c.655C>A	ENSP00000507155.1:p.Pro219Thr
ENST00000394419.9:c.655C>A MANE Select	ENSP00000377941.4:p.Pro219Thr
ENST00000679147.1:c.655C>A	ENSP00000504355.1:p.Pro219Thr
ENST00000193403.10:c.655C>A	ENSP00000193403.6:p.Pro219Thr
ENST00000376839.7:c.460C>A	ENSP00000366035.3:p.Pro154Thr
ENST00000394419.8:c.655C>A	ENSP00000377941.4:p.Pro219Thr
ENST00000438964.6:c.655C>A	ENSP00000414272.2:p.Pro219Thr
ENST00000538545.6:c.655C>A	ENSP00000439828.2:p.Pro219Thr
ENST00000554158.1:n.530C>A
ENST00000554508.5:n.348C>A
ENST00000555616.5:c.460C>A	ENSP00000450903.1:p.Pro154Thr
ENST00000556433.5:c.592C>A	ENSP00000450764.1:p.Pro198Thr
NM_001102.3:c.655C>A	NP_001093.1:p.Pro219Thr
NM_001130004.1:c.655C>A , LRG_886t1:c.655C>A	NP_001123476.1:p.Pro219Thr
NM_001130005.1:c.655C>A	NP_001123477.1:p.Pro219Thr
XM_011537265.1:c.742C>A	XP_011535567.1:p.Pro248Thr
XM_011537266.1:c.742C>A	XP_011535568.1:p.Pro248Thr
XM_011537267.1:c.742C>A	XP_011535569.1:p.Pro248Thr
XM_011537268.1:c.742C>A	XP_011535570.1:p.Pro248Thr
XM_011537269.1:c.655C>A	XP_011535571.1:p.Pro219Thr
XM_011537270.1:c.592C>A	XP_011535572.1:p.Pro198Thr
XM_011537271.1:c.592C>A	XP_011535573.1:p.Pro198Thr
XM_011537265.2:c.742C>A	XP_011535567.1:p.Pro248Thr
XM_011537266.3:c.742C>A	XP_011535568.1:p.Pro248Thr
XM_011537267.3:c.742C>A	XP_011535569.1:p.Pro248Thr
XM_011537268.3:c.742C>A	XP_011535570.1:p.Pro248Thr
XM_017021720.1:c.742C>A	XP_016877209.1:p.Pro248Thr
XM_017021721.2:c.742C>A	XP_016877210.1:p.Pro248Thr
XM_017021722.2:c.655C>A	XP_016877211.1:p.Pro219Thr
XM_017021723.2:c.655C>A	XP_016877212.1:p.Pro219Thr
XM_017021725.1:c.592C>A	XP_016877214.1:p.Pro198Thr
XM_017021726.2:c.592C>A	XP_016877215.1:p.Pro198Thr
XM_017021727.2:c.655C>A	XP_016877216.1:p.Pro219Thr
XM_017021728.2:c.592C>A	XP_016877217.1:p.Pro198Thr
NM_001102.4:c.655C>A	NP_001093.1:p.Pro219Thr
NM_001130005.2:c.655C>A	NP_001123477.1:p.Pro219Thr
NM_001130004.2:c.655C>A MANE Select	NP_001123476.1:p.Pro219Thr