Canonical Allele Identifier: CA345392645

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925890T>A (hg19) ; chr1:g.236762590T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762590T>A , CM000663.2:g.236762590T>A	GRCh38
NC_000001.10:g.236925890T>A , CM000663.1:g.236925890T>A	GRCh37
NC_000001.9:g.234992513T>A	NCBI36
NG_009081.1:g.81121T>A
NG_009081.2:g.103450T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2656T>A	ENSP00000443495.1:p.Ser886Thr
ENST00000461367.2:n.952T>A
ENST00000492634.7:n.2586T>A
ENST00000682015.1:c.2563T>A	ENSP00000506961.1:p.Ser855Thr
ENST00000682490.1:n.574T>A
ENST00000682692.1:n.3751T>A
ENST00000682966.1:n.8297T>A
ENST00000683111.1:c.*1942T>A	ENSP00000507913.1:n.*1942T>A
ENST00000683322.1:n.4008T>A
ENST00000683805.1:n.1447T>A
ENST00000684050.1:n.5294T>A
ENST00000684122.1:n.2090T>A
ENST00000684286.1:n.4211T>A
ENST00000684502.1:n.3953T>A
ENST00000684763.1:n.1271T>A
ENST00000366578.6:c.2656T>A MANE Select	ENSP00000355537.4:p.Ser886Thr
ENST00000492634.6:n.2586T>A
ENST00000542672.6:c.2656T>A	ENSP00000443495.1:p.Ser886Thr
ENST00000651091.1:c.2346T>A	ENSP00000498677.1:n.2346T>A
ENST00000651275.1:c.2548T>A	ENSP00000498926.1:p.Ser850Thr
ENST00000651781.1:c.1736T>A
ENST00000651786.1:c.*2028T>A	ENSP00000498364.1:n.*2028T>A
ENST00000652096.1:c.*2061T>A	ENSP00000498896.1:n.*2061T>A
ENST00000366578.5:c.2656T>A	ENSP00000355537.4:p.Ser886Thr
ENST00000542672.5:c.2656T>A	ENSP00000443495.1:p.Ser886Thr
ENST00000546208.5:c.2032T>A	ENSP00000438384.2:p.Ser678Thr
NM_001103.3:c.2656T>A	NP_001094.1:p.Ser886Thr
NM_001278343.1:c.2656T>A	NP_001265272.1:p.Ser886Thr
NM_001278344.1:c.2032T>A	NP_001265273.1:p.Ser678Thr
NM_001278343.2:c.2656T>A	NP_001265272.1:p.Ser886Thr
NM_001103.4:c.2656T>A MANE Select	NP_001094.1:p.Ser886Thr
NM_001278344.2:c.2032T>A	NP_001265273.1:p.Ser678Thr