Canonical Allele Identifier: CA1981509739
Gene: NADSYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71483570G= , CM000673.2:g.71483570G= GRCh38
NC_000011.9:g.71194616G= , CM000673.1:g.71194616G= GRCh37
NC_000011.8:g.70872264G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000319023.7:c.1319+553G= MANE Select ENSP00000326424.2:n.1319+553G=
ENST00000319023.6:c.1319+553G= ENSP00000326424.2:n.1319+553G=
ENST00000524450.1:n.295+553G=
ENST00000525200.5:c.2625+553G=
ENST00000526039.6:n.494+553G=
ENST00000529840.5:c.206+553G= ENSP00000437172.1:n.206+553G=
ENST00000530055.5:c.206+553G= ENSP00000431820.1:n.206+553G=
ENST00000531236.1:n.1384+553G=
NM_018161.4:c.1319+553G= NP_060631.2:n.1319+553G=
NM_018161.5:c.1319+553G= MANE Select NP_060631.2:n.1319+553G=
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