Canonical Allele Identifier: CA405693550

Gene: ACTN4

Linked Data

• MyVariant Identifiers: chr19:g.39198823C>A (hg19) ; chr19:g.38708183C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708183C>A , CM000681.2:g.38708183C>A	GRCh38
NC_000019.9:g.39198823C>A , CM000681.1:g.39198823C>A	GRCh37
NC_000019.8:g.43890663C>A	NCBI36
NG_007082.2:g.65497C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.639C>A	ENSP00000398393.2:p.Asp213Glu
ENST00000697712.1:c.498C>A	ENSP00000513410.1:p.Asp166Glu
ENST00000252699.7:c.639C>A MANE Select	ENSP00000252699.2:p.Asp213Glu
ENST00000424234.7:c.639C>A	ENSP00000411187.4:p.Asp213Glu
ENST00000440400.2:c.639C>A	ENSP00000398393.2:p.Asp213Glu
ENST00000252699.6:c.639C>A	ENSP00000252699.2:p.Asp213Glu
ENST00000390009.7:c.163-6286C>A	ENSP00000439497.1:n.163-6286C>A
ENST00000424234.6:c.272+7474C>A	ENSP00000411187.3:n.272+7474C>A
ENST00000495553.1:n.545C>A
ENST00000586538.1:c.42C>A	ENSP00000465176.1:p.Asp14Glu
ENST00000588618.5:n.736C>A
ENST00000589528.1:c.285+7469C>A
NM_004924.4:c.639C>A	NP_004915.2:p.Asp213Glu
XM_005259281.3:c.639C>A	XP_005259338.1:p.Asp213Glu
XM_005259282.3:c.639C>A	XP_005259339.1:p.Asp213Glu
XM_006723406.1:c.639C>A	XP_006723469.1:p.Asp213Glu
NM_001322033.1:c.639C>A	NP_001308962.1:p.Asp213Glu
NM_004924.5:c.639C>A	NP_004915.2:p.Asp213Glu
XM_005259281.5:c.639C>A	XP_005259338.1:p.Asp213Glu
XM_006723406.3:c.639C>A	XP_006723469.1:p.Asp213Glu
XM_017027331.2:c.639C>A	XP_016882820.1:p.Asp213Glu
XR_001753937.1:n.123-6019G>T
NM_004924.6:c.639C>A MANE Select	NP_004915.2:p.Asp213Glu
NM_001322033.2:c.639C>A	NP_001308962.1:p.Asp213Glu