Canonical Allele Identifier: CA2335156692

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38710298A= , CM000681.2:g.38710298A=	GRCh38
NC_000019.9:g.39200938A= , CM000681.1:g.39200938A=	GRCh37
NC_000019.8:g.43892778A=	NCBI36
NG_007082.2:g.67612A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000440400.3:c.733+822A=	ENSP00000398393.2:n.733+822A=
ENST00000697712.1:c.634A=	ENSP00000513410.1:p.Thr212=
ENST00000252699.7:c.775A= MANE Select	ENSP00000252699.2:p.Thr259=
ENST00000424234.7:c.733+822A=	ENSP00000411187.4:n.733+822A=
ENST00000440400.2:c.733+822A=	ENSP00000398393.2:n.733+822A=
ENST00000252699.6:c.775A=	ENSP00000252699.2:p.Thr259=
ENST00000390009.7:c.163-4171A=	ENSP00000439497.1:n.163-4171A=
ENST00000424234.6:c.272+9589A=	ENSP00000411187.3:n.272+9589A=
ENST00000586538.1:c.136+822A=	ENSP00000465176.1:n.136+822A=
ENST00000588618.5:n.872A=
ENST00000589528.1:c.285+9584A=
NM_004924.4:c.775A=	NP_004915.2:p.Thr259=
XM_005259281.3:c.775A=	XP_005259338.1:p.Thr259=
XM_005259282.3:c.733+822A=	XP_005259339.1:n.733+822A=
XM_006723406.1:c.733+822A=	XP_006723469.1:n.733+822A=
NM_001322033.1:c.733+822A=	NP_001308962.1:n.733+822A=
NM_004924.5:c.775A=	NP_004915.2:p.Thr259=
XM_005259281.5:c.775A=	XP_005259338.1:p.Thr259=
XM_006723406.3:c.733+822A=	XP_006723469.1:n.733+822A=
XM_017027331.2:c.775A=	XP_016882820.1:p.Thr259=
XR_001753937.1:n.123-8134T=
NM_004924.6:c.775A= MANE Select	NP_004915.2:p.Thr259=
NM_001322033.2:c.733+822A=	NP_001308962.1:n.733+822A=