Canonical Allele Identifier: CA405706719

Gene: ACTN4

Linked Data

• MyVariant Identifiers: chr19:g.39219969A>C (hg19) ; chr19:g.38729329A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38729329A>C , CM000681.2:g.38729329A>C	GRCh38
NC_000019.9:g.39219969A>C , CM000681.1:g.39219969A>C	GRCh37
NC_000019.8:g.43911809A>C	NCBI36
NG_007082.2:g.86643A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000440400.3:c.2618A>C	ENSP00000398393.2:p.Tyr873Ser
ENST00000697712.1:c.2492A>C	ENSP00000513410.1:p.Tyr831Ser
ENST00000252699.7:c.2633A>C MANE Select	ENSP00000252699.2:p.Tyr878Ser
ENST00000424234.7:c.2633A>C	ENSP00000411187.4:p.Tyr878Ser
ENST00000440400.2:c.2618A>C	ENSP00000398393.2:p.Tyr873Ser
ENST00000252699.6:c.2633A>C	ENSP00000252699.2:p.Tyr878Ser
ENST00000390009.7:c.1976A>C	ENSP00000439497.1:p.Tyr659Ser
ENST00000424234.6:c.1463A>C	ENSP00000411187.3:p.Tyr488Ser
ENST00000440400.1:c.926A>C	ENSP00000398393.1:p.Tyr309Ser
ENST00000477174.1:n.452A>C
ENST00000497637.5:n.386A>C
ENST00000589528.1:c.286-660A>C
NM_004924.4:c.2633A>C	NP_004915.2:p.Tyr878Ser
XM_005259281.3:c.2618A>C	XP_005259338.1:p.Tyr873Ser
XM_005259282.3:c.2618A>C	XP_005259339.1:p.Tyr873Ser
XM_006723406.1:c.2633A>C	XP_006723469.1:p.Tyr878Ser
NM_001322033.1:c.2618A>C	NP_001308962.1:p.Tyr873Ser
NM_004924.5:c.2633A>C	NP_004915.2:p.Tyr878Ser
XM_005259281.5:c.2618A>C	XP_005259338.1:p.Tyr873Ser
XM_006723406.3:c.2633A>C	XP_006723469.1:p.Tyr878Ser
XM_017027331.2:c.2699A>C	XP_016882820.1:p.Tyr900Ser
NM_004924.6:c.2633A>C MANE Select	NP_004915.2:p.Tyr878Ser
NM_001322033.2:c.2618A>C	NP_001308962.1:p.Tyr873Ser