Canonical Allele Identifier: CA405693108
Gene: ACTN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38708149T>A , CM000681.2:g.38708149T>A GRCh38
NC_000019.9:g.39198789T>A , CM000681.1:g.39198789T>A GRCh37
NC_000019.8:g.43890629T>A NCBI36
NG_007082.2:g.65463T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000440400.3:c.605T>A ENSP00000398393.2:p.Ile202Asn
ENST00000697712.1:c.464T>A ENSP00000513410.1:p.Ile155Asn
ENST00000252699.7:c.605T>A MANE Select ENSP00000252699.2:p.Ile202Asn
ENST00000424234.7:c.605T>A ENSP00000411187.4:p.Ile202Asn
ENST00000440400.2:c.605T>A ENSP00000398393.2:p.Ile202Asn
ENST00000252699.6:c.605T>A ENSP00000252699.2:p.Ile202Asn
ENST00000390009.7:c.163-6320T>A ENSP00000439497.1:n.163-6320T>A
ENST00000424234.6:c.272+7440T>A ENSP00000411187.3:n.272+7440T>A
ENST00000495553.1:n.511T>A
ENST00000586538.1:c.8T>A ENSP00000465176.1:p.Ile3Asn
ENST00000588618.5:n.702T>A
ENST00000589528.1:c.285+7435T>A
NM_004924.4:c.605T>A NP_004915.2:p.Ile202Asn
XM_005259281.3:c.605T>A XP_005259338.1:p.Ile202Asn
XM_005259282.3:c.605T>A XP_005259339.1:p.Ile202Asn
XM_006723406.1:c.605T>A XP_006723469.1:p.Ile202Asn
NM_001322033.1:c.605T>A NP_001308962.1:p.Ile202Asn
NM_004924.5:c.605T>A NP_004915.2:p.Ile202Asn
XM_005259281.5:c.605T>A XP_005259338.1:p.Ile202Asn
XM_006723406.3:c.605T>A XP_006723469.1:p.Ile202Asn
XM_017027331.2:c.605T>A XP_016882820.1:p.Ile202Asn
XR_001753937.1:n.123-5985A>T
NM_004924.6:c.605T>A MANE Select NP_004915.2:p.Ile202Asn
NM_001322033.2:c.605T>A NP_001308962.1:p.Ile202Asn