Canonical Allele Identifier: CA2406550302
Gene: NAGA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066531C= , CM000684.2:g.42066531C= GRCh38
NC_000022.10:g.42462535C= , CM000684.1:g.42462535C= GRCh37
NC_000022.9:g.40792481C= NCBI36
NG_009247.1:g.9312G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.597+179G= MANE Select ENSP00000379680.3:n.597+179G=
ENST00000396398.7:c.597+179G= ENSP00000379680.3:n.597+179G=
ENST00000402937.1:c.597+179G= ENSP00000384603.1:n.597+179G=
ENST00000403363.5:c.597+179G= ENSP00000385283.1:n.597+179G=
NM_000262.2:c.597+179G= NP_000253.1:n.597+179G=
XM_005261615.3:c.597+179G= XP_005261672.1:n.597+179G=
XM_005261616.3:c.597+179G= XP_005261673.1:n.597+179G=
NM_001362848.1:c.597+179G= NP_001349777.1:n.597+179G=
NM_001362850.1:c.597+179G= NP_001349779.1:n.597+179G=
NM_000262.3:c.597+179G= MANE Select NP_000253.1:n.597+179G=
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