Canonical Allele Identifier: CA2576774258

Gene: ACTN4

Linked Data

• dbSNP Id: rs2145118807

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38729433G>A , CM000681.2:g.38729433G>A	GRCh38
NC_000019.9:g.39220073G>A , CM000681.1:g.39220073G>A	GRCh37
NC_000019.8:g.43911913G>A	NCBI36
NG_007082.2:g.86747G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000440400.3:c.*1G>A	ENSP00000398393.2:n.*1G>A
ENST00000697712.1:c.2596G>A	ENSP00000513410.1:n.2596G>A
ENST00000252699.7:c.*1G>A MANE Select	ENSP00000252699.2:n.*1G>A
ENST00000424234.7:c.*1G>A	ENSP00000411187.4:n.*1G>A
ENST00000440400.2:c.*1G>A	ENSP00000398393.2:n.*1G>A
ENST00000252699.6:c.*1G>A	ENSP00000252699.2:n.*1G>A
ENST00000390009.7:c.*1G>A	ENSP00000439497.1:n.*1G>A
ENST00000440400.1:c.1030G>A	ENSP00000398393.1:n.1030G>A
ENST00000497637.5:n.490G>A
ENST00000589528.1:c.286-556G>A
NM_004924.4:c.*1G>A	NP_004915.2:n.*1G>A
XM_005259281.3:c.*1G>A	XP_005259338.1:n.*1G>A
XM_005259282.3:c.*1G>A	XP_005259339.1:n.*1G>A
XM_006723406.1:c.*1G>A	XP_006723469.1:n.*1G>A
NM_001322033.1:c.*1G>A	NP_001308962.1:n.*1G>A
NM_004924.5:c.*1G>A	NP_004915.2:n.*1G>A
XM_005259281.5:c.*1G>A	XP_005259338.1:n.*1G>A
XM_006723406.3:c.*1G>A	XP_006723469.1:n.*1G>A
XM_017027331.2:c.*1G>A	XP_016882820.1:n.*1G>A
NM_004924.6:c.*1G>A MANE Select	NP_004915.2:n.*1G>A
NM_001322033.2:c.*1G>A	NP_001308962.1:n.*1G>A