Canonical Allele Identifier: CA405693187

Gene: ACTN4

Linked Data

• MyVariant Identifiers: chr19:g.39198792A>G (hg19) ; chr19:g.38708152A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708152A>G , CM000681.2:g.38708152A>G	GRCh38
NC_000019.9:g.39198792A>G , CM000681.1:g.39198792A>G	GRCh37
NC_000019.8:g.43890632A>G	NCBI36
NG_007082.2:g.65466A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.608A>G	ENSP00000398393.2:p.His203Arg
ENST00000697712.1:c.467A>G	ENSP00000513410.1:p.His156Arg
ENST00000252699.7:c.608A>G MANE Select	ENSP00000252699.2:p.His203Arg
ENST00000424234.7:c.608A>G	ENSP00000411187.4:p.His203Arg
ENST00000440400.2:c.608A>G	ENSP00000398393.2:p.His203Arg
ENST00000252699.6:c.608A>G	ENSP00000252699.2:p.His203Arg
ENST00000390009.7:c.163-6317A>G	ENSP00000439497.1:n.163-6317A>G
ENST00000424234.6:c.272+7443A>G	ENSP00000411187.3:n.272+7443A>G
ENST00000495553.1:n.514A>G
ENST00000586538.1:c.11A>G	ENSP00000465176.1:p.His4Arg
ENST00000588618.5:n.705A>G
ENST00000589528.1:c.285+7438A>G
NM_004924.4:c.608A>G	NP_004915.2:p.His203Arg
XM_005259281.3:c.608A>G	XP_005259338.1:p.His203Arg
XM_005259282.3:c.608A>G	XP_005259339.1:p.His203Arg
XM_006723406.1:c.608A>G	XP_006723469.1:p.His203Arg
NM_001322033.1:c.608A>G	NP_001308962.1:p.His203Arg
NM_004924.5:c.608A>G	NP_004915.2:p.His203Arg
XM_005259281.5:c.608A>G	XP_005259338.1:p.His203Arg
XM_006723406.3:c.608A>G	XP_006723469.1:p.His203Arg
XM_017027331.2:c.608A>G	XP_016882820.1:p.His203Arg
XR_001753937.1:n.123-5988T>C
NM_004924.6:c.608A>G MANE Select	NP_004915.2:p.His203Arg
NM_001322033.2:c.608A>G	NP_001308962.1:p.His203Arg