Canonical Allele Identifier: CA345392497

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925858T>A (hg19) ; chr1:g.236762558T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762558T>A , CM000663.2:g.236762558T>A	GRCh38
NC_000001.10:g.236925858T>A , CM000663.1:g.236925858T>A	GRCh37
NC_000001.9:g.234992481T>A	NCBI36
NG_009081.1:g.81089T>A
NG_009081.2:g.103418T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2624T>A	ENSP00000443495.1:p.Val875Glu
ENST00000461367.2:n.920T>A
ENST00000492634.7:n.2554T>A
ENST00000682015.1:c.2531T>A	ENSP00000506961.1:p.Val844Glu
ENST00000682490.1:n.542T>A
ENST00000682692.1:n.3719T>A
ENST00000682966.1:n.8265T>A
ENST00000683111.1:c.*1910T>A	ENSP00000507913.1:n.*1910T>A
ENST00000683322.1:n.3976T>A
ENST00000683805.1:n.1415T>A
ENST00000684050.1:n.5262T>A
ENST00000684122.1:n.2058T>A
ENST00000684286.1:n.4179T>A
ENST00000684502.1:n.3921T>A
ENST00000684763.1:n.1239T>A
ENST00000366578.6:c.2624T>A MANE Select	ENSP00000355537.4:p.Val875Glu
ENST00000492634.6:n.2554T>A
ENST00000542672.6:c.2624T>A	ENSP00000443495.1:p.Val875Glu
ENST00000651091.1:c.2314T>A	ENSP00000498677.1:n.2314T>A
ENST00000651275.1:c.2516T>A	ENSP00000498926.1:p.Val839Glu
ENST00000651781.1:c.1704T>A
ENST00000651786.1:c.*1996T>A	ENSP00000498364.1:n.*1996T>A
ENST00000652096.1:c.*2029T>A	ENSP00000498896.1:n.*2029T>A
ENST00000366578.5:c.2624T>A	ENSP00000355537.4:p.Val875Glu
ENST00000461367.1:n.833T>A
ENST00000542672.5:c.2624T>A	ENSP00000443495.1:p.Val875Glu
ENST00000546208.5:c.2000T>A	ENSP00000438384.2:p.Val667Glu
NM_001103.3:c.2624T>A	NP_001094.1:p.Val875Glu
NM_001278343.1:c.2624T>A	NP_001265272.1:p.Val875Glu
NM_001278344.1:c.2000T>A	NP_001265273.1:p.Val667Glu
NM_001278343.2:c.2624T>A	NP_001265272.1:p.Val875Glu
NM_001103.4:c.2624T>A MANE Select	NP_001094.1:p.Val875Glu
NM_001278344.2:c.2000T>A	NP_001265273.1:p.Val667Glu