Canonical Allele Identifier: CA10263609
Gene: NAGA HGNC NCBI

Linked Data

ClinVar Variation Id: 1382047
ClinVar RCV Id: RCV001922126
dbSNP Id: rs199980021
ExAC: 22:42456944 C / T
gnomAD v2: 22-42456944-C-T
gnomAD v3: 22-42060940-C-T
gnomAD v4: 22-42060940-C-T
MyVariant Identifiers: chr22:g.42456944C>T (hg19) chr22:g.42060940C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42060940C>T , CM000684.2:g.42060940C>T GRCh38
NC_000022.10:g.42456944C>T , CM000684.1:g.42456944C>T GRCh37
NC_000022.9:g.40786890C>T NCBI36
NG_009247.1:g.14903G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396398.8:c.1085G>A MANE Select ENSP00000379680.3:p.Gly362Glu
ENST00000396398.7:c.1085G>A ENSP00000379680.3:p.Gly362Glu
ENST00000402937.1:c.1085G>A ENSP00000384603.1:p.Gly362Glu
ENST00000403363.5:c.1085G>A ENSP00000385283.1:p.Gly362Glu
NM_000262.2:c.1085G>A NP_000253.1:p.Gly362Glu
XM_005261615.3:c.1085G>A XP_005261672.1:p.Gly362Glu
XM_005261616.3:c.1085G>A XP_005261673.1:p.Gly362Glu
NM_001362848.1:c.1085G>A NP_001349777.1:p.Gly362Glu
NM_001362850.1:c.1085G>A NP_001349779.1:p.Gly362Glu
NM_000262.3:c.1085G>A MANE Select NP_000253.1:p.Gly362Glu
Search 100 bp 5'
Search 100 bp 3'