Canonical Allele Identifier: CA2584923785

Gene: ACTN4

Linked Data

• gnomAD v4: 19-38708291-T-TCCAGATCTGCGTGCAGAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708300_38708301insCGTGCAGAACCCAGATCTG , CM000681.2:g.38708300_38708301insCGTGCAGAACCCAGATCTG	GRCh38
NC_000019.9:g.39198940_39198941insCGTGCAGAACCCAGATCTG , CM000681.1:g.39198940_39198941insCGTGCAGAACCCAGATCTG	GRCh37
NC_000019.8:g.43890780_43890781insCGTGCAGAACCCAGATCTG	NCBI36
NG_007082.2:g.65614_65615insCGTGCAGAACCCAGATCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.651+105_651+106insCGTGCAGAACCCAGATCTG	ENSP00000398393.2:n.651+105_651+106insCGTGCAGAACCCAGATCTG
ENST00000697712.1:c.510+105_510+106insCGTGCAGAACCCAGATCTG	ENSP00000513410.1:n.510+105_510+106insCGTGCAGAACCCAGATCTG
ENST00000252699.7:c.651+105_651+106insCGTGCAGAACCCAGATCTG MANE Select	ENSP00000252699.2:n.651+105_651+106insCGTGCAGAACCCAGATCTG
ENST00000424234.7:c.651+105_651+106insCGTGCAGAACCCAGATCTG	ENSP00000411187.4:n.651+105_651+106insCGTGCAGAACCCAGATCTG
ENST00000440400.2:c.651+105_651+106insCGTGCAGAACCCAGATCTG	ENSP00000398393.2:n.651+105_651+106insCGTGCAGAACCCAGATCTG
ENST00000252699.6:c.651+105_651+106insCGTGCAGAACCCAGATCTG	ENSP00000252699.2:n.651+105_651+106insCGTGCAGAACCCAGATCTG
ENST00000390009.7:c.163-6169_163-6168insCGTGCAGAACCCAGATCTG	ENSP00000439497.1:n.163-6169_163-6168insCGTGCAGAACCCAGATCTG
ENST00000424234.6:c.272+7591_272+7592insCGTGCAGAACCCAGATCTG	ENSP00000411187.3:n.272+7591_272+7592insCGTGCAGAACCCAGATCTG
ENST00000495553.1:n.557+105_557+106insCGTGCAGAACCCAGATCTG
ENST00000586538.1:c.54+105_54+106insCGTGCAGAACCCAGATCTG	ENSP00000465176.1:n.54+105_54+106insCGTGCAGAACCCAGATCTG
ENST00000588618.5:n.748+105_748+106insCGTGCAGAACCCAGATCTG
ENST00000589528.1:c.285+7586_285+7587insCGTGCAGAACCCAGATCTG
NM_004924.4:c.651+105_651+106insCGTGCAGAACCCAGATCTG	NP_004915.2:n.651+105_651+106insCGTGCAGAACCCAGATCTG
XM_005259281.3:c.651+105_651+106insCGTGCAGAACCCAGATCTG	XP_005259338.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG
XM_005259282.3:c.651+105_651+106insCGTGCAGAACCCAGATCTG	XP_005259339.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG
XM_006723406.1:c.651+105_651+106insCGTGCAGAACCCAGATCTG	XP_006723469.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG
NM_001322033.1:c.651+105_651+106insCGTGCAGAACCCAGATCTG	NP_001308962.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG
NM_004924.5:c.651+105_651+106insCGTGCAGAACCCAGATCTG	NP_004915.2:n.651+105_651+106insCGTGCAGAACCCAGATCTG
XM_005259281.5:c.651+105_651+106insCGTGCAGAACCCAGATCTG	XP_005259338.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG
XM_006723406.3:c.651+105_651+106insCGTGCAGAACCCAGATCTG	XP_006723469.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG
XM_017027331.2:c.651+105_651+106insCGTGCAGAACCCAGATCTG	XP_016882820.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG
XR_001753937.1:n.123-6128_123-6127insGTTCTGCACGCAGATCTGG
NM_004924.6:c.651+105_651+106insCGTGCAGAACCCAGATCTG MANE Select	NP_004915.2:n.651+105_651+106insCGTGCAGAACCCAGATCTG
NM_001322033.2:c.651+105_651+106insCGTGCAGAACCCAGATCTG	NP_001308962.1:n.651+105_651+106insCGTGCAGAACCCAGATCTG