Canonical Allele Identifier: CA489655529
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35085750A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34793549A>T , CM000677.2:g.34793549A>T GRCh38
NC_000015.9:g.35085750A>T , CM000677.1:g.35085750A>T GRCh37
NC_000015.8:g.32873042A>T NCBI36
NG_007553.1:g.7178T>A , LRG_388:g.7178T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.256T>A (ACTC1)
ENST00000290378.6:c.150T>A (ACTC1) MANE Select ENSP00000290378.4:p.Gly50=
ENST00000647798.1:n.297T>A (ACTC1)
ENST00000648556.1:n.307T>A (ACTC1)
ENST00000650163.1:n.230T>A (ACTC1)
ENST00000290378.4:c.150T>A (ACTC1) ENSP00000290378.4:p.Gly50=
NM_005159.4:c.150T>A , LRG_388t1:c.150T>A (ACTC1) NP_005150.1:p.Gly50=
NR_120329.1:n.299+16118A>T (GJD2-DT)
NM_005159.5:c.150T>A (ACTC1) MANE Select NP_005150.1:p.Gly50=