Canonical Allele Identifier: CA423810036

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236917336T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236754036T>C , CM000663.2:g.236754036T>C	GRCh38
NC_000001.10:g.236917336T>C , CM000663.1:g.236917336T>C	GRCh37
NC_000001.9:g.234983959T>C	NCBI36
NG_009081.1:g.72567T>C
NG_009081.2:g.94896T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.1929T>C	ENSP00000443495.1:p.Ala643=
ENST00000461367.2:n.225T>C
ENST00000492634.7:n.1859T>C
ENST00000682015.1:c.1836T>C	ENSP00000506961.1:p.Ala612=
ENST00000682692.1:n.3024T>C
ENST00000682966.1:n.7570T>C
ENST00000683111.1:c.*1215T>C	ENSP00000507913.1:n.*1215T>C
ENST00000683322.1:n.3281T>C
ENST00000684050.1:n.4567T>C
ENST00000684286.1:n.3484T>C
ENST00000684502.1:n.3226T>C
ENST00000684763.1:n.544T>C
ENST00000366578.6:c.1929T>C MANE Select	ENSP00000355537.4:p.Ala643=
ENST00000492634.6:n.1859T>C
ENST00000542672.6:c.1929T>C	ENSP00000443495.1:p.Ala643=
ENST00000651091.1:c.1619T>C	ENSP00000498677.1:n.1619T>C
ENST00000651275.1:c.1821T>C	ENSP00000498926.1:p.Ala607=
ENST00000651781.1:c.1009T>C
ENST00000651786.1:c.*1301T>C	ENSP00000498364.1:n.*1301T>C
ENST00000652096.1:c.*1334T>C	ENSP00000498896.1:n.*1334T>C
ENST00000366578.5:c.1929T>C	ENSP00000355537.4:p.Ala643=
ENST00000461367.1:n.138T>C
ENST00000542672.5:c.1929T>C	ENSP00000443495.1:p.Ala643=
ENST00000546208.5:c.1305T>C	ENSP00000438384.2:p.Ala435=
NM_001103.3:c.1929T>C	NP_001094.1:p.Ala643=
NM_001278343.1:c.1929T>C	NP_001265272.1:p.Ala643=
NM_001278344.1:c.1305T>C	NP_001265273.1:p.Ala435=
NM_001278343.2:c.1929T>C	NP_001265272.1:p.Ala643=
NM_001103.4:c.1929T>C MANE Select	NP_001094.1:p.Ala643=
NM_001278344.2:c.1305T>C	NP_001265273.1:p.Ala435=