Canonical Allele Identifier: CA2657022158
Gene: NAGA HGNC NCBI

Linked Data

gnomAD v4: 22-42067072-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42067072T>G , CM000684.2:g.42067072T>G GRCh38
NC_000022.10:g.42463076T>G , CM000684.1:g.42463076T>G GRCh37
NC_000022.9:g.40793022T>G NCBI36
NG_009247.1:g.8771A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396398.8:c.502+41A>C MANE Select ENSP00000379680.3:n.502+41A>C
ENST00000396398.7:c.502+41A>C ENSP00000379680.3:n.502+41A>C
ENST00000402937.1:c.502+41A>C ENSP00000384603.1:n.502+41A>C
ENST00000403363.5:c.502+41A>C ENSP00000385283.1:n.502+41A>C
NM_000262.2:c.502+41A>C NP_000253.1:n.502+41A>C
XM_005261615.3:c.502+41A>C XP_005261672.1:n.502+41A>C
XM_005261616.3:c.502+41A>C XP_005261673.1:n.502+41A>C
NM_001362848.1:c.502+41A>C NP_001349777.1:n.502+41A>C
NM_001362850.1:c.502+41A>C NP_001349779.1:n.502+41A>C
NM_000262.3:c.502+41A>C MANE Select NP_000253.1:n.502+41A>C
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