Canonical Allele Identifier: CA345373552

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236882244G>A (hg19) ; chr1:g.236718944G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236718944G>A , CM000663.2:g.236718944G>A	GRCh38
NC_000001.10:g.236882244G>A , CM000663.1:g.236882244G>A	GRCh37
NC_000001.9:g.234948867G>A	NCBI36
NG_009081.1:g.37475G>A
NG_009081.2:g.59804G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.292G>A	ENSP00000443495.1:p.Ala98Thr
ENST00000492634.7:n.387G>A
ENST00000494762.2:n.41G>A
ENST00000682015.1:c.292G>A	ENSP00000506961.1:p.Ala98Thr
ENST00000682692.1:n.292G>A
ENST00000682966.1:n.291G>A
ENST00000683075.1:n.231G>A
ENST00000683111.1:c.235G>A	ENSP00000507913.1:p.Ala79Thr
ENST00000684050.1:n.327G>A
ENST00000684286.1:n.360G>A
ENST00000684502.1:n.327G>A
ENST00000366578.6:c.292G>A MANE Select	ENSP00000355537.4:p.Ala98Thr
ENST00000492634.6:n.387G>A
ENST00000542672.6:c.292G>A	ENSP00000443495.1:p.Ala98Thr
ENST00000651091.1:c.235G>A	ENSP00000498677.1:p.Ala79Thr
ENST00000651187.1:c.76G>A	ENSP00000498348.1:p.Ala26Thr
ENST00000651275.1:c.277G>A	ENSP00000498926.1:p.Ala93Thr
ENST00000651786.1:c.292G>A	ENSP00000498364.1:p.Ala98Thr
ENST00000652096.1:c.292G>A	ENSP00000498896.1:p.Ala98Thr
ENST00000366578.5:c.292G>A	ENSP00000355537.4:p.Ala98Thr
ENST00000492634.5:n.439G>A
ENST00000542672.5:c.292G>A	ENSP00000443495.1:p.Ala98Thr
ENST00000546208.5:c.-530G>A	ENSP00000438384.2:n.-530G>A
NM_001103.3:c.292G>A	NP_001094.1:p.Ala98Thr
NM_001278343.1:c.292G>A	NP_001265272.1:p.Ala98Thr
NM_001278344.1:c.-530G>A	NP_001265273.1:n.-530G>A
NM_001278343.2:c.292G>A	NP_001265272.1:p.Ala98Thr
NM_001103.4:c.292G>A MANE Select	NP_001094.1:p.Ala98Thr
NM_001278344.2:c.-530G>A	NP_001265273.1:n.-530G>A