Canonical Allele Identifier: CA2739268001

Gene: NAGA

Linked Data

• ClinVar Variation Id: 2847758
• ClinVar RCV Id: RCV003635218

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42063037A>G , CM000684.2:g.42063037A>G	GRCh38
NC_000022.10:g.42459041A>G , CM000684.1:g.42459041A>G	GRCh37
NC_000022.9:g.40788987A>G	NCBI36
NG_009247.1:g.12806T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.760-13T>C MANE Select	ENSP00000379680.3:n.760-13T>C
ENST00000396398.7:c.760-13T>C	ENSP00000379680.3:n.760-13T>C
ENST00000402937.1:c.760-13T>C	ENSP00000384603.1:n.760-13T>C
ENST00000403363.5:c.760-13T>C	ENSP00000385283.1:n.760-13T>C
NM_000262.2:c.760-13T>C	NP_000253.1:n.760-13T>C
XM_005261615.3:c.760-13T>C	XP_005261672.1:n.760-13T>C
XM_005261616.3:c.760-13T>C	XP_005261673.1:n.760-13T>C
NM_001362848.1:c.760-13T>C	NP_001349777.1:n.760-13T>C
NM_001362850.1:c.760-13T>C	NP_001349779.1:n.760-13T>C
NM_000262.3:c.760-13T>C MANE Select	NP_000253.1:n.760-13T>C