Canonical Allele Identifier: CA391631087

Gene: ACTC1 GJD2-DT

Linked Data

• ClinVar Variation Id: 1332337
• ClinVar RCV Id: RCV001805383
• dbSNP Id: rs2140430970
• MyVariant Identifiers: chr15:g.35084721A>T (hg19) ; chr15:g.34792520A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34792520A>T , CM000677.2:g.34792520A>T	GRCh38
NC_000015.9:g.35084721A>T , CM000677.1:g.35084721A>T	GRCh37
NC_000015.8:g.32872013A>T	NCBI36
NG_007553.1:g.8207T>A , LRG_388:g.8207T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560563.2:n.610T>A (ACTC1)
ENST00000290378.6:c.504T>A (ACTC1) MANE Select	ENSP00000290378.4:p.Tyr168Ter
ENST00000647798.1:n.598T>A (ACTC1)
ENST00000648556.1:n.661T>A (ACTC1)
ENST00000650163.1:n.584T>A (ACTC1)
ENST00000290378.4:c.504T>A (ACTC1)	ENSP00000290378.4:p.Tyr168Ter
ENST00000557860.1:n.194T>A (ACTC1)
ENST00000560563.1:n.3T>A (ACTC1)
NM_005159.4:c.504T>A , LRG_388t1:c.504T>A (ACTC1)	NP_005150.1:p.Tyr168Ter
NR_120329.1:n.299+15089A>T (GJD2-DT)
NM_005159.5:c.504T>A (ACTC1) MANE Select	NP_005150.1:p.Tyr168Ter