Canonical Allele Identifier: CA345392308
Gene: ACTN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762526G>C , CM000663.2:g.236762526G>C GRCh38
NC_000001.10:g.236925826G>C , CM000663.1:g.236925826G>C GRCh37
NC_000001.9:g.234992449G>C NCBI36
NG_009081.1:g.81057G>C
NG_009081.2:g.103386G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2592G>C ENSP00000443495.1:p.Lys864Asn
ENST00000461367.2:n.888G>C
ENST00000492634.7:n.2522G>C
ENST00000682015.1:c.2499G>C ENSP00000506961.1:p.Lys833Asn
ENST00000682490.1:n.510G>C
ENST00000682692.1:n.3687G>C
ENST00000682966.1:n.8233G>C
ENST00000683111.1:c.*1878G>C ENSP00000507913.1:n.*1878G>C
ENST00000683322.1:n.3944G>C
ENST00000683805.1:n.1383G>C
ENST00000684050.1:n.5230G>C
ENST00000684122.1:n.2026G>C
ENST00000684286.1:n.4147G>C
ENST00000684502.1:n.3889G>C
ENST00000684763.1:n.1207G>C
ENST00000366578.6:c.2592G>C MANE Select ENSP00000355537.4:p.Lys864Asn
ENST00000492634.6:n.2522G>C
ENST00000542672.6:c.2592G>C ENSP00000443495.1:p.Lys864Asn
ENST00000651091.1:c.2282G>C ENSP00000498677.1:n.2282G>C
ENST00000651275.1:c.2484G>C ENSP00000498926.1:p.Lys828Asn
ENST00000651781.1:c.1672G>C
ENST00000651786.1:c.*1964G>C ENSP00000498364.1:n.*1964G>C
ENST00000652096.1:c.*1997G>C ENSP00000498896.1:n.*1997G>C
ENST00000366578.5:c.2592G>C ENSP00000355537.4:p.Lys864Asn
ENST00000461367.1:n.801G>C
ENST00000542672.5:c.2592G>C ENSP00000443495.1:p.Lys864Asn
ENST00000546208.5:c.1968G>C ENSP00000438384.2:p.Lys656Asn
NM_001103.3:c.2592G>C NP_001094.1:p.Lys864Asn
NM_001278343.1:c.2592G>C NP_001265272.1:p.Lys864Asn
NM_001278344.1:c.1968G>C NP_001265273.1:p.Lys656Asn
NM_001278343.2:c.2592G>C NP_001265272.1:p.Lys864Asn
NM_001103.4:c.2592G>C MANE Select NP_001094.1:p.Lys864Asn
NM_001278344.2:c.1968G>C NP_001265273.1:p.Lys656Asn