Canonical Allele Identifier: CA345387102

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236917372C>A (hg19) ; chr1:g.236754072C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236754072C>A , CM000663.2:g.236754072C>A	GRCh38
NC_000001.10:g.236917372C>A , CM000663.1:g.236917372C>A	GRCh37
NC_000001.9:g.234983995C>A	NCBI36
NG_009081.1:g.72603C>A
NG_009081.2:g.94932C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.1965C>A	ENSP00000443495.1:p.Asn655Lys
ENST00000461367.2:n.261C>A
ENST00000492634.7:n.1895C>A
ENST00000682015.1:c.1872C>A	ENSP00000506961.1:p.Asn624Lys
ENST00000682692.1:n.3060C>A
ENST00000682966.1:n.7606C>A
ENST00000683111.1:c.*1251C>A	ENSP00000507913.1:n.*1251C>A
ENST00000683322.1:n.3317C>A
ENST00000684050.1:n.4603C>A
ENST00000684286.1:n.3520C>A
ENST00000684502.1:n.3262C>A
ENST00000684763.1:n.580C>A
ENST00000366578.6:c.1965C>A MANE Select	ENSP00000355537.4:p.Asn655Lys
ENST00000492634.6:n.1895C>A
ENST00000542672.6:c.1965C>A	ENSP00000443495.1:p.Asn655Lys
ENST00000651091.1:c.1655C>A	ENSP00000498677.1:n.1655C>A
ENST00000651275.1:c.1857C>A	ENSP00000498926.1:p.Asn619Lys
ENST00000651781.1:c.1045C>A
ENST00000651786.1:c.*1337C>A	ENSP00000498364.1:n.*1337C>A
ENST00000652096.1:c.*1370C>A	ENSP00000498896.1:n.*1370C>A
ENST00000366578.5:c.1965C>A	ENSP00000355537.4:p.Asn655Lys
ENST00000461367.1:n.174C>A
ENST00000542672.5:c.1965C>A	ENSP00000443495.1:p.Asn655Lys
ENST00000546208.5:c.1341C>A	ENSP00000438384.2:p.Asn447Lys
NM_001103.3:c.1965C>A	NP_001094.1:p.Asn655Lys
NM_001278343.1:c.1965C>A	NP_001265272.1:p.Asn655Lys
NM_001278344.1:c.1341C>A	NP_001265273.1:p.Asn447Lys
NM_001278343.2:c.1965C>A	NP_001265272.1:p.Asn655Lys
NM_001103.4:c.1965C>A MANE Select	NP_001094.1:p.Asn655Lys
NM_001278344.2:c.1341C>A	NP_001265273.1:p.Asn447Lys