Canonical Allele Identifier: CA2335166153
Gene: ACTN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38729335T= , CM000681.2:g.38729335T= GRCh38
NC_000019.9:g.39219975T= , CM000681.1:g.39219975T= GRCh37
NC_000019.8:g.43911815T= NCBI36
NG_007082.2:g.86649T=

Transcript Alleles

HGVS Amino-acid change
ENST00000440400.3:c.2624T= ENSP00000398393.2:p.Ile875=
ENST00000697712.1:c.2498T= ENSP00000513410.1:p.Ile833=
ENST00000252699.7:c.2639T= MANE Select ENSP00000252699.2:p.Ile880=
ENST00000424234.7:c.2639T= ENSP00000411187.4:p.Ile880=
ENST00000440400.2:c.2624T= ENSP00000398393.2:p.Ile875=
ENST00000252699.6:c.2639T= ENSP00000252699.2:p.Ile880=
ENST00000390009.7:c.1982T= ENSP00000439497.1:p.Ile661=
ENST00000424234.6:c.1469T= ENSP00000411187.3:p.Ile490=
ENST00000440400.1:c.932T= ENSP00000398393.1:p.Ile311=
ENST00000477174.1:n.458T=
ENST00000497637.5:n.392T=
ENST00000589528.1:c.286-654T=
NM_004924.4:c.2639T= NP_004915.2:p.Ile880=
XM_005259281.3:c.2624T= XP_005259338.1:p.Ile875=
XM_005259282.3:c.2624T= XP_005259339.1:p.Ile875=
XM_006723406.1:c.2639T= XP_006723469.1:p.Ile880=
NM_001322033.1:c.2624T= NP_001308962.1:p.Ile875=
NM_004924.5:c.2639T= NP_004915.2:p.Ile880=
XM_005259281.5:c.2624T= XP_005259338.1:p.Ile875=
XM_006723406.3:c.2639T= XP_006723469.1:p.Ile880=
XM_017027331.2:c.2705T= XP_016882820.1:p.Ile902=
NM_004924.6:c.2639T= MANE Select NP_004915.2:p.Ile880=
NM_001322033.2:c.2624T= NP_001308962.1:p.Ile875=