Canonical Allele Identifier: CA345387135

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236917378G>T (hg19) ; chr1:g.236754078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236754078G>T , CM000663.2:g.236754078G>T	GRCh38
NC_000001.10:g.236917378G>T , CM000663.1:g.236917378G>T	GRCh37
NC_000001.9:g.234984001G>T	NCBI36
NG_009081.1:g.72609G>T
NG_009081.2:g.94938G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.1971G>T	ENSP00000443495.1:p.Met657Ile
ENST00000461367.2:n.267G>T
ENST00000492634.7:n.1901G>T
ENST00000682015.1:c.1878G>T	ENSP00000506961.1:p.Met626Ile
ENST00000682692.1:n.3066G>T
ENST00000682966.1:n.7612G>T
ENST00000683111.1:c.*1257G>T	ENSP00000507913.1:n.*1257G>T
ENST00000683322.1:n.3323G>T
ENST00000684050.1:n.4609G>T
ENST00000684286.1:n.3526G>T
ENST00000684502.1:n.3268G>T
ENST00000684763.1:n.586G>T
ENST00000366578.6:c.1971G>T MANE Select	ENSP00000355537.4:p.Met657Ile
ENST00000492634.6:n.1901G>T
ENST00000542672.6:c.1971G>T	ENSP00000443495.1:p.Met657Ile
ENST00000651091.1:c.1661G>T	ENSP00000498677.1:n.1661G>T
ENST00000651275.1:c.1863G>T	ENSP00000498926.1:p.Met621Ile
ENST00000651781.1:c.1051G>T
ENST00000651786.1:c.*1343G>T	ENSP00000498364.1:n.*1343G>T
ENST00000652096.1:c.*1376G>T	ENSP00000498896.1:n.*1376G>T
ENST00000366578.5:c.1971G>T	ENSP00000355537.4:p.Met657Ile
ENST00000461367.1:n.180G>T
ENST00000542672.5:c.1971G>T	ENSP00000443495.1:p.Met657Ile
ENST00000546208.5:c.1347G>T	ENSP00000438384.2:p.Met449Ile
NM_001103.3:c.1971G>T	NP_001094.1:p.Met657Ile
NM_001278343.1:c.1971G>T	NP_001265272.1:p.Met657Ile
NM_001278344.1:c.1347G>T	NP_001265273.1:p.Met449Ile
NM_001278343.2:c.1971G>T	NP_001265272.1:p.Met657Ile
NM_001103.4:c.1971G>T MANE Select	NP_001094.1:p.Met657Ile
NM_001278344.2:c.1347G>T	NP_001265273.1:p.Met449Ile