Canonical Allele Identifier: CA2406550388
Gene: NAGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066708A= , CM000684.2:g.42066708A= GRCh38
NC_000022.10:g.42462712A= , CM000684.1:g.42462712A= GRCh37
NC_000022.9:g.40792658A= NCBI36
NG_009247.1:g.9135T=

Transcript Alleles

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