Canonical Allele Identifier: CA486981473

Gene: ACTN1

Linked Data

• MyVariant Identifiers: chr14:g.69371448A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68904731A>G , CM000676.2:g.68904731A>G	GRCh38
NC_000014.8:g.69371448A>G , CM000676.1:g.69371448A>G	GRCh37
NC_000014.7:g.68441201A>G	NCBI36
NG_029480.1:g.79636T>C , LRG_886:g.79636T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554508.6:c.405T>C	ENSP00000507578.1:p.Asp135=
ENST00000682130.1:n.888T>C
ENST00000682291.1:c.600T>C	ENSP00000507093.1:p.Asp200=
ENST00000682298.1:n.888T>C
ENST00000682331.1:c.600T>C	ENSP00000508329.1:p.Asp200=
ENST00000682378.1:n.888T>C
ENST00000682381.1:n.888T>C
ENST00000682522.1:n.489T>C
ENST00000682559.1:c.*53T>C	ENSP00000507271.1:n.*53T>C
ENST00000683069.1:n.800T>C
ENST00000683198.1:c.600T>C	ENSP00000507889.1:p.Asp200=
ENST00000683225.1:c.405T>C	ENSP00000506977.1:p.Asp135=
ENST00000683261.1:n.888T>C
ENST00000683267.1:c.600T>C	ENSP00000508356.1:p.Asp200=
ENST00000683342.1:c.600T>C	ENSP00000508301.1:p.Asp200=
ENST00000683780.1:n.1446T>C
ENST00000684096.1:n.1059T>C
ENST00000684146.1:n.888T>C
ENST00000684182.1:c.405T>C	ENSP00000508177.1:p.Asp135=
ENST00000684340.1:n.888T>C
ENST00000684598.1:c.600T>C	ENSP00000507785.1:p.Asp200=
ENST00000684638.1:c.600T>C	ENSP00000507609.1:p.Asp200=
ENST00000684639.1:c.480T>C	ENSP00000507653.1:p.Asp160=
ENST00000684713.1:c.600T>C	ENSP00000507155.1:p.Asp200=
ENST00000394419.9:c.600T>C MANE Select	ENSP00000377941.4:p.Asp200=
ENST00000679147.1:c.600T>C	ENSP00000504355.1:p.Asp200=
ENST00000193403.10:c.600T>C	ENSP00000193403.6:p.Asp200=
ENST00000376839.7:c.405T>C	ENSP00000366035.3:p.Asp135=
ENST00000394419.8:c.600T>C	ENSP00000377941.4:p.Asp200=
ENST00000438964.6:c.600T>C	ENSP00000414272.2:p.Asp200=
ENST00000538545.6:c.600T>C	ENSP00000439828.2:p.Asp200=
ENST00000553370.5:c.405T>C	ENSP00000450925.1:p.Asp135=
ENST00000554158.1:n.475T>C
ENST00000554508.5:n.293T>C
ENST00000555616.5:c.405T>C	ENSP00000450903.1:p.Asp135=
ENST00000556433.5:c.537T>C	ENSP00000450764.1:p.Asp179=
NM_001102.3:c.600T>C	NP_001093.1:p.Asp200=
NM_001130004.1:c.600T>C , LRG_886t1:c.600T>C	NP_001123476.1:p.Asp200=
NM_001130005.1:c.600T>C	NP_001123477.1:p.Asp200=
XM_011537265.1:c.687T>C	XP_011535567.1:p.Asp229=
XM_011537266.1:c.687T>C	XP_011535568.1:p.Asp229=
XM_011537267.1:c.687T>C	XP_011535569.1:p.Asp229=
XM_011537268.1:c.687T>C	XP_011535570.1:p.Asp229=
XM_011537269.1:c.600T>C	XP_011535571.1:p.Asp200=
XM_011537270.1:c.537T>C	XP_011535572.1:p.Asp179=
XM_011537271.1:c.537T>C	XP_011535573.1:p.Asp179=
XM_011537265.2:c.687T>C	XP_011535567.1:p.Asp229=
XM_011537266.3:c.687T>C	XP_011535568.1:p.Asp229=
XM_011537267.3:c.687T>C	XP_011535569.1:p.Asp229=
XM_011537268.3:c.687T>C	XP_011535570.1:p.Asp229=
XM_017021720.1:c.687T>C	XP_016877209.1:p.Asp229=
XM_017021721.2:c.687T>C	XP_016877210.1:p.Asp229=
XM_017021722.2:c.600T>C	XP_016877211.1:p.Asp200=
XM_017021723.2:c.600T>C	XP_016877212.1:p.Asp200=
XM_017021725.1:c.537T>C	XP_016877214.1:p.Asp179=
XM_017021726.2:c.537T>C	XP_016877215.1:p.Asp179=
XM_017021727.2:c.600T>C	XP_016877216.1:p.Asp200=
XM_017021728.2:c.537T>C	XP_016877217.1:p.Asp179=
NM_001102.4:c.600T>C	NP_001093.1:p.Asp200=
NM_001130005.2:c.600T>C	NP_001123477.1:p.Asp200=
NM_001130004.2:c.600T>C MANE Select	NP_001123476.1:p.Asp200=