Canonical Allele Identifier: CA1981496882
Gene: NADSYN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71456361A= , CM000673.2:g.71456361A= GRCh38
NC_000011.9:g.71167407A= , CM000673.1:g.71167407A= GRCh37
NC_000011.8:g.70845055A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000319023.7:c.146+1191A= MANE Select ENSP00000326424.2:n.146+1191A=
ENST00000319023.6:c.146+1191A= ENSP00000326424.2:n.146+1191A=
ENST00000524949.5:n.212+1191A=
ENST00000525200.5:c.46+1191A=
ENST00000525245.1:n.87+1191A=
ENST00000527538.5:n.202+1191A=
ENST00000528509.5:c.146+1191A= ENSP00000433472.1:n.146+1191A=
ENST00000529120.5:c.146+1191A= ENSP00000437220.1:n.146+1191A=
ENST00000533769.5:n.212+1191A=
ENST00000534634.5:n.334+1191A=
NM_018161.4:c.146+1191A= NP_060631.2:n.146+1191A=
NM_018161.5:c.146+1191A= MANE Select NP_060631.2:n.146+1191A=