Canonical Allele Identifier: CA2335156642

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38710203C= , CM000681.2:g.38710203C=	GRCh38
NC_000019.9:g.39200843C= , CM000681.1:g.39200843C=	GRCh37
NC_000019.8:g.43892683C=	NCBI36
NG_007082.2:g.67517C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000440400.3:c.733+727C=	ENSP00000398393.2:n.733+727C=
ENST00000697712.1:c.593-54C=	ENSP00000513410.1:n.593-54C=
ENST00000252699.7:c.734-54C= MANE Select	ENSP00000252699.2:n.734-54C=
ENST00000424234.7:c.733+727C=	ENSP00000411187.4:n.733+727C=
ENST00000440400.2:c.733+727C=	ENSP00000398393.2:n.733+727C=
ENST00000252699.6:c.734-54C=	ENSP00000252699.2:n.734-54C=
ENST00000390009.7:c.163-4266C=	ENSP00000439497.1:n.163-4266C=
ENST00000424234.6:c.272+9494C=	ENSP00000411187.3:n.272+9494C=
ENST00000586538.1:c.136+727C=	ENSP00000465176.1:n.136+727C=
ENST00000588618.5:n.831-54C=
ENST00000589528.1:c.285+9489C=
NM_004924.4:c.734-54C=	NP_004915.2:n.734-54C=
XM_005259281.3:c.734-54C=	XP_005259338.1:n.734-54C=
XM_005259282.3:c.733+727C=	XP_005259339.1:n.733+727C=
XM_006723406.1:c.733+727C=	XP_006723469.1:n.733+727C=
NM_001322033.1:c.733+727C=	NP_001308962.1:n.733+727C=
NM_004924.5:c.734-54C=	NP_004915.2:n.734-54C=
XM_005259281.5:c.734-54C=	XP_005259338.1:n.734-54C=
XM_006723406.3:c.733+727C=	XP_006723469.1:n.733+727C=
XM_017027331.2:c.734-54C=	XP_016882820.1:n.734-54C=
XR_001753937.1:n.123-8039G=
NM_004924.6:c.734-54C= MANE Select	NP_004915.2:n.734-54C=
NM_001322033.2:c.733+727C=	NP_001308962.1:n.733+727C=