Canonical Allele Identifier: CA1025941929
Gene: NAGA HGNC NCBI

Linked Data

dbSNP Id: rs1926348671

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42061020dup , CM000684.2:g.42061020dup GRCh38
NC_000022.10:g.42457024dup , CM000684.1:g.42457024dup GRCh37
NC_000022.9:g.40786970dup NCBI36
NG_009247.1:g.14823dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.1005dup MANE Select ENSP00000379680.3:p.Ser336Ter
ENST00000396398.7:c.1005dup ENSP00000379680.3:p.Ser336Ter
ENST00000402937.1:c.1005dup ENSP00000384603.1:p.Ser336Ter
ENST00000403363.5:c.1005dup ENSP00000385283.1:p.Ser336Ter
NM_000262.2:c.1005dup NP_000253.1:p.Ser336Ter
XM_005261615.3:c.1005dup XP_005261672.1:p.Ser336Ter
XM_005261616.3:c.1005dup XP_005261673.1:p.Ser336Ter
NM_001362848.1:c.1005dup NP_001349777.1:p.Ser336Ter
NM_001362850.1:c.1005dup NP_001349779.1:p.Ser336Ter
NM_000262.3:c.1005dup MANE Select NP_000253.1:p.Ser336Ter