Canonical Allele Identifier: CA1981498695
Gene: NADSYN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71459957G= , CM000673.2:g.71459957G= GRCh38
NC_000011.9:g.71171003G= , CM000673.1:g.71171003G= GRCh37
NC_000011.8:g.70848651G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000319023.7:c.263+1413G= MANE Select ENSP00000326424.2:n.263+1413G=
ENST00000319023.6:c.263+1413G= ENSP00000326424.2:n.263+1413G=
ENST00000524949.5:n.329+1413G=
ENST00000525200.5:c.163+1413G=
ENST00000525245.1:n.205-84G=
ENST00000527538.5:n.602G=
ENST00000528509.5:c.263+1413G= ENSP00000433472.1:n.263+1413G=
ENST00000529120.5:c.*8+1401G= ENSP00000437220.1:n.*8+1401G=
ENST00000533769.5:n.329+1413G=
NM_018161.4:c.263+1413G= NP_060631.2:n.263+1413G=
NM_018161.5:c.263+1413G= MANE Select NP_060631.2:n.263+1413G=