Canonical Allele Identifier: CA2335166152
Gene: ACTN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38729334A= , CM000681.2:g.38729334A= GRCh38
NC_000019.9:g.39219974A= , CM000681.1:g.39219974A= GRCh37
NC_000019.8:g.43911814A= NCBI36
NG_007082.2:g.86648A=

Transcript Alleles

HGVS Amino-acid change
ENST00000440400.3:c.2623A= ENSP00000398393.2:p.Ile875=
ENST00000697712.1:c.2497A= ENSP00000513410.1:p.Ile833=
ENST00000252699.7:c.2638A= MANE Select ENSP00000252699.2:p.Ile880=
ENST00000424234.7:c.2638A= ENSP00000411187.4:p.Ile880=
ENST00000440400.2:c.2623A= ENSP00000398393.2:p.Ile875=
ENST00000252699.6:c.2638A= ENSP00000252699.2:p.Ile880=
ENST00000390009.7:c.1981A= ENSP00000439497.1:p.Ile661=
ENST00000424234.6:c.1468A= ENSP00000411187.3:p.Ile490=
ENST00000440400.1:c.931A= ENSP00000398393.1:p.Ile311=
ENST00000477174.1:n.457A=
ENST00000497637.5:n.391A=
ENST00000589528.1:c.286-655A=
NM_004924.4:c.2638A= NP_004915.2:p.Ile880=
XM_005259281.3:c.2623A= XP_005259338.1:p.Ile875=
XM_005259282.3:c.2623A= XP_005259339.1:p.Ile875=
XM_006723406.1:c.2638A= XP_006723469.1:p.Ile880=
NM_001322033.1:c.2623A= NP_001308962.1:p.Ile875=
NM_004924.5:c.2638A= NP_004915.2:p.Ile880=
XM_005259281.5:c.2623A= XP_005259338.1:p.Ile875=
XM_006723406.3:c.2638A= XP_006723469.1:p.Ile880=
XM_017027331.2:c.2704A= XP_016882820.1:p.Ile902=
NM_004924.6:c.2638A= MANE Select NP_004915.2:p.Ile880=
NM_001322033.2:c.2623A= NP_001308962.1:p.Ile875=