Canonical Allele Identifier: CA2335156602

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38710114_38710121delinsTGGCTGAG , CM000681.2:g.38710114_38710121delinsTGGCTGAG	GRCh38
NC_000019.9:g.39200754_39200761delinsTGGCTGAG , CM000681.1:g.39200754_39200761delinsTGGCTGAG	GRCh37
NC_000019.8:g.43892594_43892601delinsTGGCTGAG	NCBI36
NG_007082.2:g.67428_67435delinsTGGCTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.733+638_733+645delinsTGGCTGAG	ENSP00000398393.2:n.733+638_733+645delinsTGGCTGAG
ENST00000697712.1:c.593-143_593-136delinsTGGCTGAG	ENSP00000513410.1:n.593-143_593-136delinsTGGCTGAG
ENST00000252699.7:c.734-143_734-136delinsTGGCTGAG MANE Select	ENSP00000252699.2:n.734-143_734-136delinsTGGCTGAG
ENST00000424234.7:c.733+638_733+645delinsTGGCTGAG	ENSP00000411187.4:n.733+638_733+645delinsTGGCTGAG
ENST00000440400.2:c.733+638_733+645delinsTGGCTGAG	ENSP00000398393.2:n.733+638_733+645delinsTGGCTGAG
ENST00000252699.6:c.734-143_734-136delinsTGGCTGAG	ENSP00000252699.2:n.734-143_734-136delinsTGGCTGAG
ENST00000390009.7:c.163-4355_163-4348delinsTGGCTGAG	ENSP00000439497.1:n.163-4355_163-4348delinsTGGCTGAG
ENST00000424234.6:c.272+9405_272+9412delinsTGGCTGAG	ENSP00000411187.3:n.272+9405_272+9412delinsTGGCTGAG
ENST00000586538.1:c.136+638_136+645delinsTGGCTGAG	ENSP00000465176.1:n.136+638_136+645delinsTGGCTGAG
ENST00000588618.5:n.831-143_831-136delinsTGGCTGAG
ENST00000589528.1:c.285+9400_285+9407delinsTGGCTGAG
NM_004924.4:c.734-143_734-136delinsTGGCTGAG	NP_004915.2:n.734-143_734-136delinsTGGCTGAG
XM_005259281.3:c.734-143_734-136delinsTGGCTGAG	XP_005259338.1:n.734-143_734-136delinsTGGCTGAG
XM_005259282.3:c.733+638_733+645delinsTGGCTGAG	XP_005259339.1:n.733+638_733+645delinsTGGCTGAG
XM_006723406.1:c.733+638_733+645delinsTGGCTGAG	XP_006723469.1:n.733+638_733+645delinsTGGCTGAG
NM_001322033.1:c.733+638_733+645delinsTGGCTGAG	NP_001308962.1:n.733+638_733+645delinsTGGCTGAG
NM_004924.5:c.734-143_734-136delinsTGGCTGAG	NP_004915.2:n.734-143_734-136delinsTGGCTGAG
XM_005259281.5:c.734-143_734-136delinsTGGCTGAG	XP_005259338.1:n.734-143_734-136delinsTGGCTGAG
XM_006723406.3:c.733+638_733+645delinsTGGCTGAG	XP_006723469.1:n.733+638_733+645delinsTGGCTGAG
XM_017027331.2:c.734-143_734-136delinsTGGCTGAG	XP_016882820.1:n.734-143_734-136delinsTGGCTGAG
XR_001753937.1:n.123-7957_123-7950delinsCTCAGCCA
NM_004924.6:c.734-143_734-136delinsTGGCTGAG MANE Select	NP_004915.2:n.734-143_734-136delinsTGGCTGAG
NM_001322033.2:c.733+638_733+645delinsTGGCTGAG	NP_001308962.1:n.733+638_733+645delinsTGGCTGAG