Canonical Allele Identifier: CA753285007

Gene: NAGA

Linked Data

• dbSNP Id: rs1339266615
• gnomAD v3: 22-42061242-CT-C
• gnomAD v4: 22-42061242-CT-C
• MyVariant Identifiers: chr22:g.42457247del (hg19) ; chr22:g.42061243del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42061244del , CM000684.2:g.42061244del	GRCh38
NC_000022.10:g.42457248del , CM000684.1:g.42457248del	GRCh37
NC_000022.9:g.40787194del	NCBI36
NG_009247.1:g.14600del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.958-176del MANE Select	ENSP00000379680.3:n.958-176del
ENST00000396398.7:c.958-176del	ENSP00000379680.3:n.958-176del
ENST00000402937.1:c.958-176del	ENSP00000384603.1:n.958-176del
ENST00000403363.5:c.958-176del	ENSP00000385283.1:n.958-176del
NM_000262.2:c.958-176del	NP_000253.1:n.958-176del
XM_005261615.3:c.958-176del	XP_005261672.1:n.958-176del
XM_005261616.3:c.958-176del	XP_005261673.1:n.958-176del
NM_001362848.1:c.958-176del	NP_001349777.1:n.958-176del
NM_001362850.1:c.958-176del	NP_001349779.1:n.958-176del
NM_000262.3:c.958-176del MANE Select	NP_000253.1:n.958-176del