Canonical Allele Identifier: CA2335166198

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38729435C= , CM000681.2:g.38729435C=	GRCh38
NC_000019.9:g.39220075C= , CM000681.1:g.39220075C=	GRCh37
NC_000019.8:g.43911915C=	NCBI36
NG_007082.2:g.86749C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.*3C=	ENSP00000398393.2:n.*3C=
ENST00000697712.1:c.2598C=	ENSP00000513410.1:n.2598C=
ENST00000252699.7:c.*3C= MANE Select	ENSP00000252699.2:n.*3C=
ENST00000424234.7:c.*3C=	ENSP00000411187.4:n.*3C=
ENST00000440400.2:c.*3C=	ENSP00000398393.2:n.*3C=
ENST00000252699.6:c.*3C=	ENSP00000252699.2:n.*3C=
ENST00000390009.7:c.*3C=	ENSP00000439497.1:n.*3C=
ENST00000440400.1:c.1032C=	ENSP00000398393.1:n.1032C=
ENST00000497637.5:n.492C=
ENST00000589528.1:c.286-554C=
NM_004924.4:c.*3C=	NP_004915.2:n.*3C=
XM_005259281.3:c.*3C=	XP_005259338.1:n.*3C=
XM_005259282.3:c.*3C=	XP_005259339.1:n.*3C=
XM_006723406.1:c.*3C=	XP_006723469.1:n.*3C=
NM_001322033.1:c.*3C=	NP_001308962.1:n.*3C=
NM_004924.5:c.*3C=	NP_004915.2:n.*3C=
XM_005259281.5:c.*3C=	XP_005259338.1:n.*3C=
XM_006723406.3:c.*3C=	XP_006723469.1:n.*3C=
XM_017027331.2:c.*3C=	XP_016882820.1:n.*3C=
NM_004924.6:c.*3C= MANE Select	NP_004915.2:n.*3C=
NM_001322033.2:c.*3C=	NP_001308962.1:n.*3C=