Canonical Allele Identifier: CA2584924130
Gene: ACTN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38710210A>G , CM000681.2:g.38710210A>G GRCh38
NC_000019.9:g.39200850A>G , CM000681.1:g.39200850A>G GRCh37
NC_000019.8:g.43892690A>G NCBI36
NG_007082.2:g.67524A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000440400.3:c.733+734A>G ENSP00000398393.2:n.733+734A>G
ENST00000697712.1:c.593-47A>G ENSP00000513410.1:n.593-47A>G
ENST00000252699.7:c.734-47A>G MANE Select ENSP00000252699.2:n.734-47A>G
ENST00000424234.7:c.733+734A>G ENSP00000411187.4:n.733+734A>G
ENST00000440400.2:c.733+734A>G ENSP00000398393.2:n.733+734A>G
ENST00000252699.6:c.734-47A>G ENSP00000252699.2:n.734-47A>G
ENST00000390009.7:c.163-4259A>G ENSP00000439497.1:n.163-4259A>G
ENST00000424234.6:c.272+9501A>G ENSP00000411187.3:n.272+9501A>G
ENST00000586538.1:c.136+734A>G ENSP00000465176.1:n.136+734A>G
ENST00000588618.5:n.831-47A>G
ENST00000589528.1:c.285+9496A>G
NM_004924.4:c.734-47A>G NP_004915.2:n.734-47A>G
XM_005259281.3:c.734-47A>G XP_005259338.1:n.734-47A>G
XM_005259282.3:c.733+734A>G XP_005259339.1:n.733+734A>G
XM_006723406.1:c.733+734A>G XP_006723469.1:n.733+734A>G
NM_001322033.1:c.733+734A>G NP_001308962.1:n.733+734A>G
NM_004924.5:c.734-47A>G NP_004915.2:n.734-47A>G
XM_005259281.5:c.734-47A>G XP_005259338.1:n.734-47A>G
XM_006723406.3:c.733+734A>G XP_006723469.1:n.733+734A>G
XM_017027331.2:c.734-47A>G XP_016882820.1:n.734-47A>G
XR_001753937.1:n.123-8046T>C
NM_004924.6:c.734-47A>G MANE Select NP_004915.2:n.734-47A>G
NM_001322033.2:c.733+734A>G NP_001308962.1:n.733+734A>G