Canonical Allele Identifier: CA12790588

Gene: NKAIN3

Linked Data

• dbSNP Id: rs2882926
• gnomAD v2: 8-63621569-A-T
• gnomAD v3: 8-62709010-A-T
• gnomAD v4: 8-62709010-A-T
• MyVariant Identifiers: chr8:g.63621569A>T (hg19) ; chr8:g.62709010A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.62709010A>T , CM000670.2:g.62709010A>T	GRCh38
NC_000008.10:g.63621569A>T , CM000670.1:g.63621569A>T	GRCh37
NC_000008.9:g.63784123A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519049.6:c.274-37922A>T	ENSP00000501734.1:n.274-37922A>T
ENST00000623646.3:c.274-37922A>T MANE Select	ENSP00000501908.1:n.274-37922A>T
ENST00000674732.1:c.274-37922A>T	ENSP00000501789.1:n.274-37922A>T
ENST00000674746.1:c.274-37922A>T	ENSP00000502044.1:n.274-37922A>T
ENST00000674864.1:c.274-37922A>T	ENSP00000502526.1:n.274-37922A>T
ENST00000674873.1:n.234-37922A>T
ENST00000675749.1:c.274-37922A>T	ENSP00000502179.1:n.274-37922A>T
ENST00000519049.5:n.663-37922A>T
ENST00000523211.5:c.274-37922A>T	ENSP00000429073.1:n.274-37922A>T
ENST00000523367.1:n.679-37922A>T
ENST00000524201.1:c.193-37922A>T	ENSP00000429393.1:n.193-37922A>T
NM_001304533.1:c.274-37922A>T	NP_001291462.1:n.274-37922A>T
NR_130764.1:n.406-37922A>T
XM_011517511.1:c.274-37922A>T	XP_011515813.1:n.274-37922A>T
XM_011517512.1:c.274-37922A>T	XP_011515814.1:n.274-37922A>T
XM_011517511.2:c.274-37922A>T	XP_011515813.1:n.274-37922A>T
XM_011517512.2:c.274-37922A>T	XP_011515814.1:n.274-37922A>T
XM_017013359.1:c.274-37922A>T	XP_016868848.1:n.274-37922A>T
XM_017013360.1:c.274-37922A>T	XP_016868849.1:n.274-37922A>T
XM_017013361.2:c.88-37922A>T	XP_016868850.1:n.88-37922A>T
NM_001304533.2:c.274-37922A>T	NP_001291462.1:n.274-37922A>T
NR_130764.2:n.494-37922A>T
NM_001304533.3:c.274-37922A>T MANE Select	NP_001291462.1:n.274-37922A>T