Canonical Allele Identifier: CA2335155802

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708425T= , CM000681.2:g.38708425T=	GRCh38
NC_000019.9:g.39199065T= , CM000681.1:g.39199065T=	GRCh37
NC_000019.8:g.43890905T=	NCBI36
NG_007082.2:g.65739T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.651+230T=	ENSP00000398393.2:n.651+230T=
ENST00000697712.1:c.510+230T=	ENSP00000513410.1:n.510+230T=
ENST00000252699.7:c.651+230T= MANE Select	ENSP00000252699.2:n.651+230T=
ENST00000424234.7:c.651+230T=	ENSP00000411187.4:n.651+230T=
ENST00000440400.2:c.651+230T=	ENSP00000398393.2:n.651+230T=
ENST00000252699.6:c.651+230T=	ENSP00000252699.2:n.651+230T=
ENST00000390009.7:c.163-6044T=	ENSP00000439497.1:n.163-6044T=
ENST00000424234.6:c.272+7716T=	ENSP00000411187.3:n.272+7716T=
ENST00000495553.1:n.557+230T=
ENST00000586538.1:c.54+230T=	ENSP00000465176.1:n.54+230T=
ENST00000588618.5:n.748+230T=
ENST00000589528.1:c.285+7711T=
NM_004924.4:c.651+230T=	NP_004915.2:n.651+230T=
XM_005259281.3:c.651+230T=	XP_005259338.1:n.651+230T=
XM_005259282.3:c.651+230T=	XP_005259339.1:n.651+230T=
XM_006723406.1:c.651+230T=	XP_006723469.1:n.651+230T=
NM_001322033.1:c.651+230T=	NP_001308962.1:n.651+230T=
NM_004924.5:c.651+230T=	NP_004915.2:n.651+230T=
XM_005259281.5:c.651+230T=	XP_005259338.1:n.651+230T=
XM_006723406.3:c.651+230T=	XP_006723469.1:n.651+230T=
XM_017027331.2:c.651+230T=	XP_016882820.1:n.651+230T=
XR_001753937.1:n.123-6261A=
NM_004924.6:c.651+230T= MANE Select	NP_004915.2:n.651+230T=
NM_001322033.2:c.651+230T=	NP_001308962.1:n.651+230T=