Canonical Allele Identifier: CA2814352244

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708359G>T , CM000681.2:g.38708359G>T	GRCh38
NC_000019.9:g.39198999G>T , CM000681.1:g.39198999G>T	GRCh37
NC_000019.8:g.43890839G>T	NCBI36
NG_007082.2:g.65673G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.651+164G>T	ENSP00000398393.2:n.651+164G>T
ENST00000697712.1:c.510+164G>T	ENSP00000513410.1:n.510+164G>T
ENST00000252699.7:c.651+164G>T MANE Select	ENSP00000252699.2:n.651+164G>T
ENST00000424234.7:c.651+164G>T	ENSP00000411187.4:n.651+164G>T
ENST00000440400.2:c.651+164G>T	ENSP00000398393.2:n.651+164G>T
ENST00000252699.6:c.651+164G>T	ENSP00000252699.2:n.651+164G>T
ENST00000390009.7:c.163-6110G>T	ENSP00000439497.1:n.163-6110G>T
ENST00000424234.6:c.272+7650G>T	ENSP00000411187.3:n.272+7650G>T
ENST00000495553.1:n.557+164G>T
ENST00000586538.1:c.54+164G>T	ENSP00000465176.1:n.54+164G>T
ENST00000588618.5:n.748+164G>T
ENST00000589528.1:c.285+7645G>T
NM_004924.4:c.651+164G>T	NP_004915.2:n.651+164G>T
XM_005259281.3:c.651+164G>T	XP_005259338.1:n.651+164G>T
XM_005259282.3:c.651+164G>T	XP_005259339.1:n.651+164G>T
XM_006723406.1:c.651+164G>T	XP_006723469.1:n.651+164G>T
NM_001322033.1:c.651+164G>T	NP_001308962.1:n.651+164G>T
NM_004924.5:c.651+164G>T	NP_004915.2:n.651+164G>T
XM_005259281.5:c.651+164G>T	XP_005259338.1:n.651+164G>T
XM_006723406.3:c.651+164G>T	XP_006723469.1:n.651+164G>T
XM_017027331.2:c.651+164G>T	XP_016882820.1:n.651+164G>T
XR_001753937.1:n.123-6195C>A
NM_004924.6:c.651+164G>T MANE Select	NP_004915.2:n.651+164G>T
NM_001322033.2:c.651+164G>T	NP_001308962.1:n.651+164G>T