Canonical Allele Identifier: CA423807016

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236882309T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236719009T>C , CM000663.2:g.236719009T>C	GRCh38
NC_000001.10:g.236882309T>C , CM000663.1:g.236882309T>C	GRCh37
NC_000001.9:g.234948932T>C	NCBI36
NG_009081.1:g.37540T>C
NG_009081.2:g.59869T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.357T>C	ENSP00000443495.1:p.Ala119=
ENST00000492634.7:n.452T>C
ENST00000494762.2:n.106T>C
ENST00000682015.1:c.357T>C	ENSP00000506961.1:p.Ala119=
ENST00000682692.1:n.357T>C
ENST00000682966.1:n.356T>C
ENST00000683075.1:n.296T>C
ENST00000683111.1:c.300T>C	ENSP00000507913.1:p.Ala100=
ENST00000684050.1:n.392T>C
ENST00000684286.1:n.425T>C
ENST00000684502.1:n.392T>C
ENST00000366578.6:c.357T>C MANE Select	ENSP00000355537.4:p.Ala119=
ENST00000492634.6:n.452T>C
ENST00000542672.6:c.357T>C	ENSP00000443495.1:p.Ala119=
ENST00000651091.1:c.300T>C	ENSP00000498677.1:p.Ala100=
ENST00000651187.1:c.141T>C	ENSP00000498348.1:p.Ala47=
ENST00000651275.1:c.342T>C	ENSP00000498926.1:p.Ala114=
ENST00000651786.1:c.357T>C	ENSP00000498364.1:p.Ala119=
ENST00000652096.1:c.357T>C	ENSP00000498896.1:p.Ala119=
ENST00000366578.5:c.357T>C	ENSP00000355537.4:p.Ala119=
ENST00000492634.5:n.504T>C
ENST00000542672.5:c.357T>C	ENSP00000443495.1:p.Ala119=
ENST00000546208.5:c.-465T>C	ENSP00000438384.2:n.-465T>C
NM_001103.3:c.357T>C	NP_001094.1:p.Ala119=
NM_001278343.1:c.357T>C	NP_001265272.1:p.Ala119=
NM_001278344.1:c.-465T>C	NP_001265273.1:n.-465T>C
NM_001278343.2:c.357T>C	NP_001265272.1:p.Ala119=
NM_001103.4:c.357T>C MANE Select	NP_001094.1:p.Ala119=
NM_001278344.2:c.-465T>C	NP_001265273.1:n.-465T>C