Canonical Allele Identifier: CA1788600303

Gene: NKAIN3

Linked Data

• dbSNP Id: rs1585707218

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.62346089T>G , CM000670.2:g.62346089T>G	GRCh38
NC_000008.10:g.63258648T>G , CM000670.1:g.63258648T>G	GRCh37
NC_000008.9:g.63421202T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519049.6:c.54+96962T>G	ENSP00000501734.1:n.54+96962T>G
ENST00000623646.3:c.54+96962T>G MANE Select	ENSP00000501908.1:n.54+96962T>G
ENST00000674732.1:c.54+96962T>G	ENSP00000501789.1:n.54+96962T>G
ENST00000674746.1:c.54+96962T>G	ENSP00000502044.1:n.54+96962T>G
ENST00000674864.1:c.54+96962T>G	ENSP00000502526.1:n.54+96962T>G
ENST00000675749.1:c.54+96962T>G	ENSP00000502179.1:n.54+96962T>G
ENST00000519049.5:n.443+96962T>G
ENST00000523211.5:c.54+96962T>G	ENSP00000429073.1:n.54+96962T>G
ENST00000523367.1:n.459+96962T>G
ENST00000524201.1:c.54+96962T>G	ENSP00000429393.1:n.54+96962T>G
NM_001304533.1:c.54+96962T>G	NP_001291462.1:n.54+96962T>G
NR_130764.1:n.186+96962T>G
XM_011517511.1:c.54+96962T>G	XP_011515813.1:n.54+96962T>G
XM_011517512.1:c.54+96962T>G	XP_011515814.1:n.54+96962T>G
XM_011517513.1:c.54+96962T>G	XP_011515815.1:n.54+96962T>G
XM_011517511.2:c.54+96962T>G	XP_011515813.1:n.54+96962T>G
XM_011517512.2:c.54+96962T>G	XP_011515814.1:n.54+96962T>G
XM_017013359.1:c.54+96962T>G	XP_016868848.1:n.54+96962T>G
XM_017013360.1:c.54+96962T>G	XP_016868849.1:n.54+96962T>G
NM_001304533.2:c.54+96962T>G	NP_001291462.1:n.54+96962T>G
NR_130764.2:n.274+96962T>G
NM_001304533.3:c.54+96962T>G MANE Select	NP_001291462.1:n.54+96962T>G