Canonical Allele Identifier: CA2724367983
Gene: NADSYN1 HGNC NCBI

Linked Data

dbSNP Id: rs2120481081

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71483420A>G , CM000673.2:g.71483420A>G GRCh38
NC_000011.9:g.71194466A>G , CM000673.1:g.71194466A>G GRCh37
NC_000011.8:g.70872114A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000319023.7:c.1319+403A>G MANE Select ENSP00000326424.2:n.1319+403A>G
ENST00000319023.6:c.1319+403A>G ENSP00000326424.2:n.1319+403A>G
ENST00000524450.1:n.295+403A>G
ENST00000525200.5:c.2625+403A>G
ENST00000526039.6:n.494+403A>G
ENST00000529840.5:c.206+403A>G ENSP00000437172.1:n.206+403A>G
ENST00000530055.5:c.206+403A>G ENSP00000431820.1:n.206+403A>G
ENST00000531236.1:n.1384+403A>G
NM_018161.4:c.1319+403A>G NP_060631.2:n.1319+403A>G
NM_018161.5:c.1319+403A>G MANE Select NP_060631.2:n.1319+403A>G