Canonical Allele Identifier: CA405693065

Gene: ACTN4

Linked Data

• MyVariant Identifiers: chr19:g.39198783C>A (hg19) ; chr19:g.38708143C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708143C>A , CM000681.2:g.38708143C>A	GRCh38
NC_000019.9:g.39198783C>A , CM000681.1:g.39198783C>A	GRCh37
NC_000019.8:g.43890623C>A	NCBI36
NG_007082.2:g.65457C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000440400.3:c.599C>A	ENSP00000398393.2:p.Ala200Asp
ENST00000697712.1:c.458C>A	ENSP00000513410.1:p.Ala153Asp
ENST00000252699.7:c.599C>A MANE Select	ENSP00000252699.2:p.Ala200Asp
ENST00000424234.7:c.599C>A	ENSP00000411187.4:p.Ala200Asp
ENST00000440400.2:c.599C>A	ENSP00000398393.2:p.Ala200Asp
ENST00000252699.6:c.599C>A	ENSP00000252699.2:p.Ala200Asp
ENST00000390009.7:c.163-6326C>A	ENSP00000439497.1:n.163-6326C>A
ENST00000424234.6:c.272+7434C>A	ENSP00000411187.3:n.272+7434C>A
ENST00000495553.1:n.505C>A
ENST00000586538.1:c.2C>A	ENSP00000465176.1:p.Ala1Asp
ENST00000588618.5:n.696C>A
ENST00000589528.1:c.285+7429C>A
NM_004924.4:c.599C>A	NP_004915.2:p.Ala200Asp
XM_005259281.3:c.599C>A	XP_005259338.1:p.Ala200Asp
XM_005259282.3:c.599C>A	XP_005259339.1:p.Ala200Asp
XM_006723406.1:c.599C>A	XP_006723469.1:p.Ala200Asp
NM_001322033.1:c.599C>A	NP_001308962.1:p.Ala200Asp
NM_004924.5:c.599C>A	NP_004915.2:p.Ala200Asp
XM_005259281.5:c.599C>A	XP_005259338.1:p.Ala200Asp
XM_006723406.3:c.599C>A	XP_006723469.1:p.Ala200Asp
XM_017027331.2:c.599C>A	XP_016882820.1:p.Ala200Asp
XR_001753937.1:n.123-5979G>T
NM_004924.6:c.599C>A MANE Select	NP_004915.2:p.Ala200Asp
NM_001322033.2:c.599C>A	NP_001308962.1:p.Ala200Asp