Canonical Allele Identifier: CA639474061

Gene: NAGA

Linked Data

• dbSNP Id: rs1268970176
• gnomAD v2: 22-42457270-TCAA-T
• gnomAD v3: 22-42061266-TCAA-T
• gnomAD v4: 22-42061266-TCAA-T
• MyVariant Identifiers: chr22:g.42457271_42457273del (hg19) ; chr22:g.42061267_42061269del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42061269_42061271del , CM000684.2:g.42061269_42061271del	GRCh38
NC_000022.10:g.42457273_42457275del , CM000684.1:g.42457273_42457275del	GRCh37
NC_000022.9:g.40787219_40787221del	NCBI36
NG_009247.1:g.14574_14576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.958-202_958-200del MANE Select	ENSP00000379680.3:n.958-202_958-200del
ENST00000396398.7:c.958-202_958-200del	ENSP00000379680.3:n.958-202_958-200del
ENST00000402937.1:c.958-202_958-200del	ENSP00000384603.1:n.958-202_958-200del
ENST00000403363.5:c.958-202_958-200del	ENSP00000385283.1:n.958-202_958-200del
NM_000262.2:c.958-202_958-200del	NP_000253.1:n.958-202_958-200del
XM_005261615.3:c.958-202_958-200del	XP_005261672.1:n.958-202_958-200del
XM_005261616.3:c.958-202_958-200del	XP_005261673.1:n.958-202_958-200del
NM_001362848.1:c.958-202_958-200del	NP_001349777.1:n.958-202_958-200del
NM_001362850.1:c.958-202_958-200del	NP_001349779.1:n.958-202_958-200del
NM_000262.3:c.958-202_958-200del MANE Select	NP_000253.1:n.958-202_958-200del