Canonical Allele Identifier: CA2819057142
Gene: NAGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066550T>C , CM000684.2:g.42066550T>C GRCh38
NC_000022.10:g.42462554T>C , CM000684.1:g.42462554T>C GRCh37
NC_000022.9:g.40792500T>C NCBI36
NG_009247.1:g.9293A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396398.8:c.597+160A>G MANE Select ENSP00000379680.3:n.597+160A>G
ENST00000396398.7:c.597+160A>G ENSP00000379680.3:n.597+160A>G
ENST00000402937.1:c.597+160A>G ENSP00000384603.1:n.597+160A>G
ENST00000403363.5:c.597+160A>G ENSP00000385283.1:n.597+160A>G
NM_000262.2:c.597+160A>G NP_000253.1:n.597+160A>G
XM_005261615.3:c.597+160A>G XP_005261672.1:n.597+160A>G
XM_005261616.3:c.597+160A>G XP_005261673.1:n.597+160A>G
NM_001362848.1:c.597+160A>G NP_001349777.1:n.597+160A>G
NM_001362850.1:c.597+160A>G NP_001349779.1:n.597+160A>G
NM_000262.3:c.597+160A>G MANE Select NP_000253.1:n.597+160A>G