Canonical Allele Identifier: CA2657021980
Gene: NAGA HGNC NCBI

Linked Data

gnomAD v4: 22-42066668-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066668G>T , CM000684.2:g.42066668G>T GRCh38
NC_000022.10:g.42462672G>T , CM000684.1:g.42462672G>T GRCh37
NC_000022.9:g.40792618G>T NCBI36
NG_009247.1:g.9175C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396398.8:c.597+42C>A MANE Select ENSP00000379680.3:n.597+42C>A
ENST00000396398.7:c.597+42C>A ENSP00000379680.3:n.597+42C>A
ENST00000402937.1:c.597+42C>A ENSP00000384603.1:n.597+42C>A
ENST00000403363.5:c.597+42C>A ENSP00000385283.1:n.597+42C>A
NM_000262.2:c.597+42C>A NP_000253.1:n.597+42C>A
XM_005261615.3:c.597+42C>A XP_005261672.1:n.597+42C>A
XM_005261616.3:c.597+42C>A XP_005261673.1:n.597+42C>A
NM_001362848.1:c.597+42C>A NP_001349777.1:n.597+42C>A
NM_001362850.1:c.597+42C>A NP_001349779.1:n.597+42C>A
NM_000262.3:c.597+42C>A MANE Select NP_000253.1:n.597+42C>A
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