Canonical Allele Identifier: CA2335166151

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38729333C= , CM000681.2:g.38729333C=	GRCh38
NC_000019.9:g.39219973C= , CM000681.1:g.39219973C=	GRCh37
NC_000019.8:g.43911813C=	NCBI36
NG_007082.2:g.86647C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.2622C=	ENSP00000398393.2:p.Cys874=
ENST00000697712.1:c.2496C=	ENSP00000513410.1:p.Cys832=
ENST00000252699.7:c.2637C= MANE Select	ENSP00000252699.2:p.Cys879=
ENST00000424234.7:c.2637C=	ENSP00000411187.4:p.Cys879=
ENST00000440400.2:c.2622C=	ENSP00000398393.2:p.Cys874=
ENST00000252699.6:c.2637C=	ENSP00000252699.2:p.Cys879=
ENST00000390009.7:c.1980C=	ENSP00000439497.1:p.Cys660=
ENST00000424234.6:c.1467C=	ENSP00000411187.3:p.Cys489=
ENST00000440400.1:c.930C=	ENSP00000398393.1:p.Cys310=
ENST00000477174.1:n.456C=
ENST00000497637.5:n.390C=
ENST00000589528.1:c.286-656C=
NM_004924.4:c.2637C=	NP_004915.2:p.Cys879=
XM_005259281.3:c.2622C=	XP_005259338.1:p.Cys874=
XM_005259282.3:c.2622C=	XP_005259339.1:p.Cys874=
XM_006723406.1:c.2637C=	XP_006723469.1:p.Cys879=
NM_001322033.1:c.2622C=	NP_001308962.1:p.Cys874=
NM_004924.5:c.2637C=	NP_004915.2:p.Cys879=
XM_005259281.5:c.2622C=	XP_005259338.1:p.Cys874=
XM_006723406.3:c.2637C=	XP_006723469.1:p.Cys879=
XM_017027331.2:c.2703C=	XP_016882820.1:p.Cys901=
NM_004924.6:c.2637C= MANE Select	NP_004915.2:p.Cys879=
NM_001322033.2:c.2622C=	NP_001308962.1:p.Cys874=