Canonical Allele Identifier: CA2584923807

Gene: ACTN4

Linked Data

• gnomAD v4: 19-38708315-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708316_38708317insCT , CM000681.2:g.38708316_38708317insCT	GRCh38
NC_000019.9:g.39198956_39198957insCT , CM000681.1:g.39198956_39198957insCT	GRCh37
NC_000019.8:g.43890796_43890797insCT	NCBI36
NG_007082.2:g.65630_65631insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.651+121_651+122insCT	ENSP00000398393.2:n.651+121_651+122insCT
ENST00000697712.1:c.510+121_510+122insCT	ENSP00000513410.1:n.510+121_510+122insCT
ENST00000252699.7:c.651+121_651+122insCT MANE Select	ENSP00000252699.2:n.651+121_651+122insCT
ENST00000424234.7:c.651+121_651+122insCT	ENSP00000411187.4:n.651+121_651+122insCT
ENST00000440400.2:c.651+121_651+122insCT	ENSP00000398393.2:n.651+121_651+122insCT
ENST00000252699.6:c.651+121_651+122insCT	ENSP00000252699.2:n.651+121_651+122insCT
ENST00000390009.7:c.163-6153_163-6152insCT	ENSP00000439497.1:n.163-6153_163-6152insCT
ENST00000424234.6:c.272+7607_272+7608insCT	ENSP00000411187.3:n.272+7607_272+7608insCT
ENST00000495553.1:n.557+121_557+122insCT
ENST00000586538.1:c.54+121_54+122insCT	ENSP00000465176.1:n.54+121_54+122insCT
ENST00000588618.5:n.748+121_748+122insCT
ENST00000589528.1:c.285+7602_285+7603insCT
NM_004924.4:c.651+121_651+122insCT	NP_004915.2:n.651+121_651+122insCT
XM_005259281.3:c.651+121_651+122insCT	XP_005259338.1:n.651+121_651+122insCT
XM_005259282.3:c.651+121_651+122insCT	XP_005259339.1:n.651+121_651+122insCT
XM_006723406.1:c.651+121_651+122insCT	XP_006723469.1:n.651+121_651+122insCT
NM_001322033.1:c.651+121_651+122insCT	NP_001308962.1:n.651+121_651+122insCT
NM_004924.5:c.651+121_651+122insCT	NP_004915.2:n.651+121_651+122insCT
XM_005259281.5:c.651+121_651+122insCT	XP_005259338.1:n.651+121_651+122insCT
XM_006723406.3:c.651+121_651+122insCT	XP_006723469.1:n.651+121_651+122insCT
XM_017027331.2:c.651+121_651+122insCT	XP_016882820.1:n.651+121_651+122insCT
XR_001753937.1:n.123-6152_123-6151insGA
NM_004924.6:c.651+121_651+122insCT MANE Select	NP_004915.2:n.651+121_651+122insCT
NM_001322033.2:c.651+121_651+122insCT	NP_001308962.1:n.651+121_651+122insCT