Canonical Allele Identifier: CA345373566

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236882250G>A (hg19) ; chr1:g.236718950G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236718950G>A , CM000663.2:g.236718950G>A	GRCh38
NC_000001.10:g.236882250G>A , CM000663.1:g.236882250G>A	GRCh37
NC_000001.9:g.234948873G>A	NCBI36
NG_009081.1:g.37481G>A
NG_009081.2:g.59810G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.298G>A	ENSP00000443495.1:p.Val100Ile
ENST00000492634.7:n.393G>A
ENST00000494762.2:n.47G>A
ENST00000682015.1:c.298G>A	ENSP00000506961.1:p.Val100Ile
ENST00000682692.1:n.298G>A
ENST00000682966.1:n.297G>A
ENST00000683075.1:n.237G>A
ENST00000683111.1:c.241G>A	ENSP00000507913.1:p.Val81Ile
ENST00000684050.1:n.333G>A
ENST00000684286.1:n.366G>A
ENST00000684502.1:n.333G>A
ENST00000366578.6:c.298G>A MANE Select	ENSP00000355537.4:p.Val100Ile
ENST00000492634.6:n.393G>A
ENST00000542672.6:c.298G>A	ENSP00000443495.1:p.Val100Ile
ENST00000651091.1:c.241G>A	ENSP00000498677.1:p.Val81Ile
ENST00000651187.1:c.82G>A	ENSP00000498348.1:p.Val28Ile
ENST00000651275.1:c.283G>A	ENSP00000498926.1:p.Val95Ile
ENST00000651786.1:c.298G>A	ENSP00000498364.1:p.Val100Ile
ENST00000652096.1:c.298G>A	ENSP00000498896.1:p.Val100Ile
ENST00000366578.5:c.298G>A	ENSP00000355537.4:p.Val100Ile
ENST00000492634.5:n.445G>A
ENST00000542672.5:c.298G>A	ENSP00000443495.1:p.Val100Ile
ENST00000546208.5:c.-524G>A	ENSP00000438384.2:n.-524G>A
NM_001103.3:c.298G>A	NP_001094.1:p.Val100Ile
NM_001278343.1:c.298G>A	NP_001265272.1:p.Val100Ile
NM_001278344.1:c.-524G>A	NP_001265273.1:n.-524G>A
NM_001278343.2:c.298G>A	NP_001265272.1:p.Val100Ile
NM_001103.4:c.298G>A MANE Select	NP_001094.1:p.Val100Ile
NM_001278344.2:c.-524G>A	NP_001265273.1:n.-524G>A