Canonical Allele Identifier: CA324656060

Gene: NAGA

Linked Data

• dbSNP Id: rs765657298
• gnomAD v2: 22-42462665-G-A
• gnomAD v3: 22-42066661-G-A
• gnomAD v4: 22-42066661-G-A
• MyVariant Identifiers: chr22:g.42462665G>A (hg19) ; chr22:g.42066661G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42066661G>A , CM000684.2:g.42066661G>A	GRCh38
NC_000022.10:g.42462665G>A , CM000684.1:g.42462665G>A	GRCh37
NC_000022.9:g.40792611G>A	NCBI36
NG_009247.1:g.9182C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396398.8:c.597+49C>T MANE Select	ENSP00000379680.3:n.597+49C>T
ENST00000396398.7:c.597+49C>T	ENSP00000379680.3:n.597+49C>T
ENST00000402937.1:c.597+49C>T	ENSP00000384603.1:n.597+49C>T
ENST00000403363.5:c.597+49C>T	ENSP00000385283.1:n.597+49C>T
NM_000262.2:c.597+49C>T	NP_000253.1:n.597+49C>T
XM_005261615.3:c.597+49C>T	XP_005261672.1:n.597+49C>T
XM_005261616.3:c.597+49C>T	XP_005261673.1:n.597+49C>T
NM_001362848.1:c.597+49C>T	NP_001349777.1:n.597+49C>T
NM_001362850.1:c.597+49C>T	NP_001349779.1:n.597+49C>T
NM_000262.3:c.597+49C>T MANE Select	NP_000253.1:n.597+49C>T