Canonical Allele Identifier: CA335007

Gene: ACTN2

Linked Data

• ClinVar Variation Id: 201628
• ClinVar RCV Id: RCV000183247 ; RCV001210867
• dbSNP Id: rs794728960
• MyVariant Identifiers: chr1:g.236882305G>A (hg19) ; chr1:g.236719005G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236719005G>A , CM000663.2:g.236719005G>A	GRCh38
NC_000001.10:g.236882305G>A , CM000663.1:g.236882305G>A	GRCh37
NC_000001.9:g.234948928G>A	NCBI36
NG_009081.1:g.37536G>A
NG_009081.2:g.59865G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.353G>A	ENSP00000443495.1:p.Gly118Asp
ENST00000492634.7:n.448G>A
ENST00000494762.2:n.102G>A
ENST00000682015.1:c.353G>A	ENSP00000506961.1:p.Gly118Asp
ENST00000682692.1:n.353G>A
ENST00000682966.1:n.352G>A
ENST00000683075.1:n.292G>A
ENST00000683111.1:c.296G>A	ENSP00000507913.1:p.Gly99Asp
ENST00000684050.1:n.388G>A
ENST00000684286.1:n.421G>A
ENST00000684502.1:n.388G>A
ENST00000366578.6:c.353G>A MANE Select	ENSP00000355537.4:p.Gly118Asp
ENST00000492634.6:n.448G>A
ENST00000542672.6:c.353G>A	ENSP00000443495.1:p.Gly118Asp
ENST00000651091.1:c.296G>A	ENSP00000498677.1:p.Gly99Asp
ENST00000651187.1:c.137G>A	ENSP00000498348.1:p.Gly46Asp
ENST00000651275.1:c.338G>A	ENSP00000498926.1:p.Gly113Asp
ENST00000651786.1:c.353G>A	ENSP00000498364.1:p.Gly118Asp
ENST00000652096.1:c.353G>A	ENSP00000498896.1:p.Gly118Asp
ENST00000366578.5:c.353G>A	ENSP00000355537.4:p.Gly118Asp
ENST00000492634.5:n.500G>A
ENST00000542672.5:c.353G>A	ENSP00000443495.1:p.Gly118Asp
ENST00000546208.5:c.-469G>A	ENSP00000438384.2:n.-469G>A
NM_001103.3:c.353G>A	NP_001094.1:p.Gly118Asp
NM_001278343.1:c.353G>A	NP_001265272.1:p.Gly118Asp
NM_001278344.1:c.-469G>A	NP_001265273.1:n.-469G>A
NM_001278343.2:c.353G>A	NP_001265272.1:p.Gly118Asp
NM_001103.4:c.353G>A MANE Select	NP_001094.1:p.Gly118Asp
NM_001278344.2:c.-469G>A	NP_001265273.1:n.-469G>A