Canonical Allele Identifier: CA423811295

Gene: ACTN2

Linked Data

• dbSNP Id: rs1464244007
• gnomAD v2: 1-236926024-GA-G
• gnomAD v3: 1-236762724-GA-G
• gnomAD v4: 1-236762724-GA-G
• MyVariant Identifiers: chr1:g.236926025del (hg19) ; chr1:g.236762725del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762725del , CM000663.2:g.236762725del	GRCh38
NC_000001.10:g.236926025del , CM000663.1:g.236926025del	GRCh37
NC_000001.9:g.234992648del	NCBI36
NG_009081.1:g.81256del
NG_009081.2:g.103585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.*106del	ENSP00000443495.1:n.*106del
ENST00000461367.2:n.1087del
ENST00000492634.7:n.2721del
ENST00000682015.1:c.*106del	ENSP00000506961.1:n.*106del
ENST00000682490.1:n.709del
ENST00000682692.1:n.3886del
ENST00000682966.1:n.8432del
ENST00000683111.1:c.*2077del	ENSP00000507913.1:n.*2077del
ENST00000683322.1:n.4143del
ENST00000683805.1:n.1582del
ENST00000684050.1:n.5429del
ENST00000684122.1:n.2225del
ENST00000684286.1:n.4346del
ENST00000684502.1:n.4088del
ENST00000684763.1:n.1406del
ENST00000366578.6:c.*106del MANE Select	ENSP00000355537.4:n.*106del
ENST00000492634.6:n.2721del
ENST00000542672.6:c.*106del	ENSP00000443495.1:n.*106del
ENST00000651275.1:c.2683del	ENSP00000498926.1:n.2683del
ENST00000651781.1:c.1871del
ENST00000652096.1:c.*2196del	ENSP00000498896.1:n.*2196del
ENST00000366578.5:c.*106del	ENSP00000355537.4:n.*106del
ENST00000542672.5:c.*106del	ENSP00000443495.1:n.*106del
ENST00000546208.5:c.*106del	ENSP00000438384.2:n.*106del
NM_001103.3:c.*106del	NP_001094.1:n.*106del
NM_001278343.1:c.*106del	NP_001265272.1:n.*106del
NM_001278344.1:c.*106del	NP_001265273.1:n.*106del
NM_001278343.2:c.*106del	NP_001265272.1:n.*106del
NM_001103.4:c.*106del MANE Select	NP_001094.1:n.*106del
NM_001278344.2:c.*106del	NP_001265273.1:n.*106del