Canonical Allele Identifier: CA423806972

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236882240A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236718940A>G , CM000663.2:g.236718940A>G	GRCh38
NC_000001.10:g.236882240A>G , CM000663.1:g.236882240A>G	GRCh37
NC_000001.9:g.234948863A>G	NCBI36
NG_009081.1:g.37471A>G
NG_009081.2:g.59800A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.288A>G	ENSP00000443495.1:p.Lys96=
ENST00000492634.7:n.383A>G
ENST00000494762.2:n.37A>G
ENST00000682015.1:c.288A>G	ENSP00000506961.1:p.Lys96=
ENST00000682692.1:n.288A>G
ENST00000682966.1:n.287A>G
ENST00000683075.1:n.227A>G
ENST00000683111.1:c.231A>G	ENSP00000507913.1:p.Lys77=
ENST00000684050.1:n.323A>G
ENST00000684286.1:n.356A>G
ENST00000684502.1:n.323A>G
ENST00000366578.6:c.288A>G MANE Select	ENSP00000355537.4:p.Lys96=
ENST00000492634.6:n.383A>G
ENST00000542672.6:c.288A>G	ENSP00000443495.1:p.Lys96=
ENST00000651091.1:c.231A>G	ENSP00000498677.1:p.Lys77=
ENST00000651187.1:c.72A>G	ENSP00000498348.1:p.Lys24=
ENST00000651275.1:c.273A>G	ENSP00000498926.1:p.Lys91=
ENST00000651786.1:c.288A>G	ENSP00000498364.1:p.Lys96=
ENST00000652096.1:c.288A>G	ENSP00000498896.1:p.Lys96=
ENST00000366578.5:c.288A>G	ENSP00000355537.4:p.Lys96=
ENST00000492634.5:n.435A>G
ENST00000542672.5:c.288A>G	ENSP00000443495.1:p.Lys96=
ENST00000546208.5:c.-534A>G	ENSP00000438384.2:n.-534A>G
NM_001103.3:c.288A>G	NP_001094.1:p.Lys96=
NM_001278343.1:c.288A>G	NP_001265272.1:p.Lys96=
NM_001278344.1:c.-534A>G	NP_001265273.1:n.-534A>G
NM_001278343.2:c.288A>G	NP_001265272.1:p.Lys96=
NM_001103.4:c.288A>G MANE Select	NP_001094.1:p.Lys96=
NM_001278344.2:c.-534A>G	NP_001265273.1:n.-534A>G