Canonical Allele Identifier: CA2335155705

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708223C= , CM000681.2:g.38708223C=	GRCh38
NC_000019.9:g.39198863C= , CM000681.1:g.39198863C=	GRCh37
NC_000019.8:g.43890703C=	NCBI36
NG_007082.2:g.65537C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.651+28C=	ENSP00000398393.2:n.651+28C=
ENST00000697712.1:c.510+28C=	ENSP00000513410.1:n.510+28C=
ENST00000252699.7:c.651+28C= MANE Select	ENSP00000252699.2:n.651+28C=
ENST00000424234.7:c.651+28C=	ENSP00000411187.4:n.651+28C=
ENST00000440400.2:c.651+28C=	ENSP00000398393.2:n.651+28C=
ENST00000252699.6:c.651+28C=	ENSP00000252699.2:n.651+28C=
ENST00000390009.7:c.163-6246C=	ENSP00000439497.1:n.163-6246C=
ENST00000424234.6:c.272+7514C=	ENSP00000411187.3:n.272+7514C=
ENST00000495553.1:n.557+28C=
ENST00000586538.1:c.54+28C=	ENSP00000465176.1:n.54+28C=
ENST00000588618.5:n.748+28C=
ENST00000589528.1:c.285+7509C=
NM_004924.4:c.651+28C=	NP_004915.2:n.651+28C=
XM_005259281.3:c.651+28C=	XP_005259338.1:n.651+28C=
XM_005259282.3:c.651+28C=	XP_005259339.1:n.651+28C=
XM_006723406.1:c.651+28C=	XP_006723469.1:n.651+28C=
NM_001322033.1:c.651+28C=	NP_001308962.1:n.651+28C=
NM_004924.5:c.651+28C=	NP_004915.2:n.651+28C=
XM_005259281.5:c.651+28C=	XP_005259338.1:n.651+28C=
XM_006723406.3:c.651+28C=	XP_006723469.1:n.651+28C=
XM_017027331.2:c.651+28C=	XP_016882820.1:n.651+28C=
XR_001753937.1:n.123-6059G=
NM_004924.6:c.651+28C= MANE Select	NP_004915.2:n.651+28C=
NM_001322033.2:c.651+28C=	NP_001308962.1:n.651+28C=