Canonical Allele Identifier: CA345373457

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236882199A>T (hg19) ; chr1:g.236718899A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236718899A>T , CM000663.2:g.236718899A>T	GRCh38
NC_000001.10:g.236882199A>T , CM000663.1:g.236882199A>T	GRCh37
NC_000001.9:g.234948822A>T	NCBI36
NG_009081.1:g.37430A>T
NG_009081.2:g.59759A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.247A>T	ENSP00000443495.1:p.Arg83Trp
ENST00000492634.7:n.342A>T
ENST00000682015.1:c.247A>T	ENSP00000506961.1:p.Arg83Trp
ENST00000682692.1:n.247A>T
ENST00000682966.1:n.246A>T
ENST00000683075.1:n.186A>T
ENST00000683111.1:c.190A>T	ENSP00000507913.1:p.Arg64Trp
ENST00000684050.1:n.282A>T
ENST00000684286.1:n.315A>T
ENST00000684502.1:n.282A>T
ENST00000366578.6:c.247A>T MANE Select	ENSP00000355537.4:p.Arg83Trp
ENST00000492634.6:n.342A>T
ENST00000542672.6:c.247A>T	ENSP00000443495.1:p.Arg83Trp
ENST00000651091.1:c.190A>T	ENSP00000498677.1:p.Arg64Trp
ENST00000651187.1:c.31A>T	ENSP00000498348.1:p.Arg11Trp
ENST00000651275.1:c.232A>T	ENSP00000498926.1:p.Arg78Trp
ENST00000651786.1:c.247A>T	ENSP00000498364.1:p.Arg83Trp
ENST00000652096.1:c.247A>T	ENSP00000498896.1:p.Arg83Trp
ENST00000366578.5:c.247A>T	ENSP00000355537.4:p.Arg83Trp
ENST00000492634.5:n.394A>T
ENST00000542672.5:c.247A>T	ENSP00000443495.1:p.Arg83Trp
ENST00000546208.5:c.-575A>T	ENSP00000438384.2:n.-575A>T
NM_001103.3:c.247A>T	NP_001094.1:p.Arg83Trp
NM_001278343.1:c.247A>T	NP_001265272.1:p.Arg83Trp
NM_001278344.1:c.-575A>T	NP_001265273.1:n.-575A>T
NM_001278343.2:c.247A>T	NP_001265272.1:p.Arg83Trp
NM_001103.4:c.247A>T MANE Select	NP_001094.1:p.Arg83Trp
NM_001278344.2:c.-575A>T	NP_001265273.1:n.-575A>T