Canonical Allele Identifier: CA391629388
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

COSMIC: COSM3794088
MyVariant Identifiers: chr15:g.35083368C>G (hg19) chr15:g.34791167C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34791167C>G , CM000677.2:g.34791167C>G GRCh38
NC_000015.9:g.35083368C>G , CM000677.1:g.35083368C>G GRCh37
NC_000015.8:g.32870660C>G NCBI36
NG_007553.1:g.9560G>C , LRG_388:g.9560G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.1837G>C (ACTC1)
ENST00000290378.6:c.937G>C (ACTC1) MANE Select ENSP00000290378.4:p.Asp313His
ENST00000647798.1:n.1031G>C (ACTC1)
ENST00000650163.1:n.1017G>C (ACTC1)
ENST00000290378.4:c.937G>C (ACTC1) ENSP00000290378.4:p.Asp313His
ENST00000557860.1:n.627G>C (ACTC1)
NM_005159.4:c.937G>C , LRG_388t1:c.937G>C (ACTC1) NP_005150.1:p.Asp313His
NR_120329.1:n.299+13736C>G (GJD2-DT)
NM_005159.5:c.937G>C (ACTC1) MANE Select NP_005150.1:p.Asp313His
Search 100 bp 5'
Search 100 bp 3'