Canonical Allele Identifier: CA391631070
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35084714A>G (hg19) chr15:g.34792513A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792513A>G , CM000677.2:g.34792513A>G GRCh38
NC_000015.9:g.35084714A>G , CM000677.1:g.35084714A>G GRCh37
NC_000015.8:g.32872006A>G NCBI36
NG_007553.1:g.8214T>C , LRG_388:g.8214T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.617T>C (ACTC1)
ENST00000290378.6:c.511T>C (ACTC1) MANE Select ENSP00000290378.4:p.Tyr171His
ENST00000647798.1:n.605T>C (ACTC1)
ENST00000648556.1:n.668T>C (ACTC1)
ENST00000650163.1:n.591T>C (ACTC1)
ENST00000290378.4:c.511T>C (ACTC1) ENSP00000290378.4:p.Tyr171His
ENST00000557860.1:n.201T>C (ACTC1)
ENST00000560563.1:n.10T>C (ACTC1)
NM_005159.4:c.511T>C , LRG_388t1:c.511T>C (ACTC1) NP_005150.1:p.Tyr171His
NR_120329.1:n.299+15082A>G (GJD2-DT)
NM_005159.5:c.511T>C (ACTC1) MANE Select NP_005150.1:p.Tyr171His
Search 100 bp 5'
Search 100 bp 3'