Canonical Allele Identifier: CA920375126

Gene: NAGA

Linked Data

• dbSNP Id: rs1602490398
• gnomAD v4: 22-42060804-C-CTGCCAGAGGCCCTAAGCCCACGGCTCAGGGGAGGCCATATGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060845_42060846insGTTGCCAGAGGCCCTAAGCCCACGGCTCAGGGGAGGCCATATG , CM000684.2:g.42060845_42060846insGTTGCCAGAGGCCCTAAGCCCACGGCTCAGGGGAGGCCATATG	GRCh38
NC_000022.10:g.42456849_42456850insGTTGCCAGAGGCCCTAAGCCCACGGCTCAGGGGAGGCCATATG , CM000684.1:g.42456849_42456850insGTTGCCAGAGGCCCTAAGCCCACGGCTCAGGGGAGGCCATATG	GRCh37
NC_000022.9:g.40786795_40786796insGTTGCCAGAGGCCCTAAGCCCACGGCTCAGGGGAGGCCATATG	NCBI36
NG_009247.1:g.15038_15039insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA MANE Select	ENSP00000379680.3:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGC...
ENST00000396398.7:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	ENSP00000379680.3:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGC...
ENST00000402937.1:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	ENSP00000384603.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGC...
ENST00000403363.5:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	ENSP00000385283.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGC...
NM_000262.2:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	NP_000253.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGG...
XM_005261615.3:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	XP_005261672.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGT...
XM_005261616.3:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	XP_005261673.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGT...
NM_001362848.1:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	NP_001349777.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGT...
NM_001362850.1:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA	NP_001349779.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGT...
NM_000262.3:c.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGGCTTAGGGCCTCTGGCA MANE Select	NP_000253.1:n.1101+119_1101+120insACCATATGGCCTCCCCTGAGCCGTGGG...