Canonical Allele Identifier: CA178690215

Gene: NKAIN3

Linked Data

• dbSNP Id: rs765976553
• MyVariant Identifiers: chr8:g.63258832T>C (hg19) ; chr8:g.62346273T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.62346273T>C , CM000670.2:g.62346273T>C	GRCh38
NC_000008.10:g.63258832T>C , CM000670.1:g.63258832T>C	GRCh37
NC_000008.9:g.63421386T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519049.6:c.54+97146T>C	ENSP00000501734.1:n.54+97146T>C
ENST00000623646.3:c.54+97146T>C MANE Select	ENSP00000501908.1:n.54+97146T>C
ENST00000674732.1:c.54+97146T>C	ENSP00000501789.1:n.54+97146T>C
ENST00000674746.1:c.54+97146T>C	ENSP00000502044.1:n.54+97146T>C
ENST00000674864.1:c.54+97146T>C	ENSP00000502526.1:n.54+97146T>C
ENST00000675749.1:c.54+97146T>C	ENSP00000502179.1:n.54+97146T>C
ENST00000519049.5:n.443+97146T>C
ENST00000523211.5:c.54+97146T>C	ENSP00000429073.1:n.54+97146T>C
ENST00000523367.1:n.459+97146T>C
ENST00000524201.1:c.54+97146T>C	ENSP00000429393.1:n.54+97146T>C
NM_001304533.1:c.54+97146T>C	NP_001291462.1:n.54+97146T>C
NR_130764.1:n.186+97146T>C
XM_011517511.1:c.54+97146T>C	XP_011515813.1:n.54+97146T>C
XM_011517512.1:c.54+97146T>C	XP_011515814.1:n.54+97146T>C
XM_011517513.1:c.54+97146T>C	XP_011515815.1:n.54+97146T>C
XM_011517511.2:c.54+97146T>C	XP_011515813.1:n.54+97146T>C
XM_011517512.2:c.54+97146T>C	XP_011515814.1:n.54+97146T>C
XM_017013359.1:c.54+97146T>C	XP_016868848.1:n.54+97146T>C
XM_017013360.1:c.54+97146T>C	XP_016868849.1:n.54+97146T>C
NM_001304533.2:c.54+97146T>C	NP_001291462.1:n.54+97146T>C
NR_130764.2:n.274+97146T>C
NM_001304533.3:c.54+97146T>C MANE Select	NP_001291462.1:n.54+97146T>C