Canonical Allele Identifier: CA915951390

Gene: NAGA

Linked Data

• ClinVar Variation Id: 667287
• ClinVar RCV Id: RCV000825989
• dbSNP Id: rs1602490557
• gnomAD v4: 22-42060926-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060931_42060932del , CM000684.2:g.42060931_42060932del	GRCh38
NC_000022.10:g.42456935_42456936del , CM000684.1:g.42456935_42456936del	GRCh37
NC_000022.9:g.40786881_40786882del	NCBI36
NG_009247.1:g.14915_14916del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1097_1098del MANE Select	ENSP00000379680.3:p.Tyr366Ter
ENST00000396398.7:c.1097_1098del	ENSP00000379680.3:p.Tyr366Ter
ENST00000402937.1:c.1097_1098del	ENSP00000384603.1:p.Tyr366Ter
ENST00000403363.5:c.1097_1098del	ENSP00000385283.1:p.Tyr366Ter
NM_000262.2:c.1097_1098del	NP_000253.1:p.Tyr366Ter
XM_005261615.3:c.1097_1098del	XP_005261672.1:p.Tyr366Ter
XM_005261616.3:c.1097_1098del	XP_005261673.1:p.Tyr366Ter
NM_001362848.1:c.1097_1098del	NP_001349777.1:p.Tyr366Ter
NM_001362850.1:c.1097_1098del	NP_001349779.1:p.Tyr366Ter
NM_000262.3:c.1097_1098del MANE Select	NP_000253.1:p.Tyr366Ter