Canonical Allele Identifier: CA507247050

Gene: ACTN4

Linked Data

• MyVariant Identifiers: chr19:g.39198814T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708174T>C , CM000681.2:g.38708174T>C	GRCh38
NC_000019.9:g.39198814T>C , CM000681.1:g.39198814T>C	GRCh37
NC_000019.8:g.43890654T>C	NCBI36
NG_007082.2:g.65488T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.630T>C	ENSP00000398393.2:p.Ile210=
ENST00000697712.1:c.489T>C	ENSP00000513410.1:p.Ile163=
ENST00000252699.7:c.630T>C MANE Select	ENSP00000252699.2:p.Ile210=
ENST00000424234.7:c.630T>C	ENSP00000411187.4:p.Ile210=
ENST00000440400.2:c.630T>C	ENSP00000398393.2:p.Ile210=
ENST00000252699.6:c.630T>C	ENSP00000252699.2:p.Ile210=
ENST00000390009.7:c.163-6295T>C	ENSP00000439497.1:n.163-6295T>C
ENST00000424234.6:c.272+7465T>C	ENSP00000411187.3:n.272+7465T>C
ENST00000495553.1:n.536T>C
ENST00000586538.1:c.33T>C	ENSP00000465176.1:p.Ile11=
ENST00000588618.5:n.727T>C
ENST00000589528.1:c.285+7460T>C
NM_004924.4:c.630T>C	NP_004915.2:p.Ile210=
XM_005259281.3:c.630T>C	XP_005259338.1:p.Ile210=
XM_005259282.3:c.630T>C	XP_005259339.1:p.Ile210=
XM_006723406.1:c.630T>C	XP_006723469.1:p.Ile210=
NM_001322033.1:c.630T>C	NP_001308962.1:p.Ile210=
NM_004924.5:c.630T>C	NP_004915.2:p.Ile210=
XM_005259281.5:c.630T>C	XP_005259338.1:p.Ile210=
XM_006723406.3:c.630T>C	XP_006723469.1:p.Ile210=
XM_017027331.2:c.630T>C	XP_016882820.1:p.Ile210=
XR_001753937.1:n.123-6010A>G
NM_004924.6:c.630T>C MANE Select	NP_004915.2:p.Ile210=
NM_001322033.2:c.630T>C	NP_001308962.1:p.Ile210=