Canonical Allele Identifier: CA1114543348
Gene: NKAIN3 HGNC NCBI

Linked Data

dbSNP Id: rs1816003022
gnomAD v3: 8-62346274-T-G
gnomAD v4: 8-62346274-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.62346274T>G , CM000670.2:g.62346274T>G GRCh38
NC_000008.10:g.63258833T>G , CM000670.1:g.63258833T>G GRCh37
NC_000008.9:g.63421387T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000519049.6:c.54+97147T>G ENSP00000501734.1:n.54+97147T>G
ENST00000623646.3:c.54+97147T>G MANE Select ENSP00000501908.1:n.54+97147T>G
ENST00000674732.1:c.54+97147T>G ENSP00000501789.1:n.54+97147T>G
ENST00000674746.1:c.54+97147T>G ENSP00000502044.1:n.54+97147T>G
ENST00000674864.1:c.54+97147T>G ENSP00000502526.1:n.54+97147T>G
ENST00000675749.1:c.54+97147T>G ENSP00000502179.1:n.54+97147T>G
ENST00000519049.5:n.443+97147T>G
ENST00000523211.5:c.54+97147T>G ENSP00000429073.1:n.54+97147T>G
ENST00000523367.1:n.459+97147T>G
ENST00000524201.1:c.54+97147T>G ENSP00000429393.1:n.54+97147T>G
NM_001304533.1:c.54+97147T>G NP_001291462.1:n.54+97147T>G
NR_130764.1:n.186+97147T>G
XM_011517511.1:c.54+97147T>G XP_011515813.1:n.54+97147T>G
XM_011517512.1:c.54+97147T>G XP_011515814.1:n.54+97147T>G
XM_011517513.1:c.54+97147T>G XP_011515815.1:n.54+97147T>G
XM_011517511.2:c.54+97147T>G XP_011515813.1:n.54+97147T>G
XM_011517512.2:c.54+97147T>G XP_011515814.1:n.54+97147T>G
XM_017013359.1:c.54+97147T>G XP_016868848.1:n.54+97147T>G
XM_017013360.1:c.54+97147T>G XP_016868849.1:n.54+97147T>G
NM_001304533.2:c.54+97147T>G NP_001291462.1:n.54+97147T>G
NR_130764.2:n.274+97147T>G
NM_001304533.3:c.54+97147T>G MANE Select NP_001291462.1:n.54+97147T>G