Canonical Allele Identifier: CA2169208279
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792383T= , CM000677.2:g.34792383T= GRCh38
NC_000015.9:g.35084584T= , CM000677.1:g.35084584T= GRCh37
NC_000015.8:g.32871876T= NCBI36
NG_007553.1:g.8344A= , LRG_388:g.8344A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.722+25A= (ACTC1)
ENST00000290378.6:c.616+25A= (ACTC1) MANE Select ENSP00000290378.4:n.616+25A=
ENST00000647798.1:n.710+25A= (ACTC1)
ENST00000648556.1:n.773+25A= (ACTC1)
ENST00000650163.1:n.696+25A= (ACTC1)
ENST00000290378.4:c.616+25A= (ACTC1) ENSP00000290378.4:n.616+25A=
ENST00000557860.1:n.306+25A= (ACTC1)
ENST00000560563.1:n.115+25A= (ACTC1)
NM_005159.4:c.616+25A= , LRG_388t1:c.616+25A= (ACTC1) NP_005150.1:n.616+25A=
NR_120329.1:n.299+14952T= (GJD2-DT)
NM_005159.5:c.616+25A= (ACTC1) MANE Select NP_005150.1:n.616+25A=
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