Canonical Allele Identifier: CA2648419624

Gene: NAXE

Linked Data

• gnomAD v4: 1-156592854-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592855_156592856insAA , CM000663.2:g.156592855_156592856insAA	GRCh38
NC_000001.10:g.156562647_156562648insAA , CM000663.1:g.156562647_156562648insAA	GRCh37
NC_000001.9:g.154829271_154829272insAA	NCBI36
NG_052542.1:g.6090_6091insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.516+185_516+186insAA MANE Select	ENSP00000357218.3:n.516+185_516+186insAA
ENST00000467374.2:n.811_812insAA
ENST00000679369.1:c.405+185_405+186insAA	ENSP00000505883.1:n.405+185_405+186insAA
ENST00000679649.1:n.555+185_555+186insAA
ENST00000679702.1:c.516+185_516+186insAA	ENSP00000505913.1:n.516+185_516+186insAA
ENST00000679913.1:n.720+185_720+186insAA
ENST00000680004.1:c.516+185_516+186insAA	ENSP00000506275.1:n.516+185_516+186insAA
ENST00000680087.1:c.516+185_516+186insAA	ENSP00000505907.1:n.516+185_516+186insAA
ENST00000680269.1:c.516+185_516+186insAA	ENSP00000505899.1:n.516+185_516+186insAA
ENST00000680529.1:n.700+185_700+186insAA
ENST00000680661.1:c.516+185_516+186insAA	ENSP00000505088.1:n.516+185_516+186insAA
ENST00000681054.1:c.516+185_516+186insAA	ENSP00000506192.1:n.516+185_516+186insAA
ENST00000681523.1:c.516+185_516+186insAA	ENSP00000505349.1:n.516+185_516+186insAA
ENST00000681645.1:n.555+185_555+186insAA
ENST00000681734.1:c.516+185_516+186insAA	ENSP00000506177.1:n.516+185_516+186insAA
ENST00000681825.1:n.505_506insAA
ENST00000681922.1:n.740_741insAA
ENST00000368233.3:c.516+185_516+186insAA	ENSP00000357216.3:n.516+185_516+186insAA
ENST00000368234.7:c.516+185_516+186insAA	ENSP00000357217.3:n.516+185_516+186insAA
ENST00000368235.7:c.516+185_516+186insAA	ENSP00000357218.3:n.516+185_516+186insAA
ENST00000467374.1:n.610_611insAA
NM_144772.2:c.516+185_516+186insAA	NP_658985.2:n.516+185_516+186insAA
XM_017000319.2:c.516+185_516+186insAA	XP_016855808.1:n.516+185_516+186insAA
NM_144772.3:c.516+185_516+186insAA MANE Select	NP_658985.2:n.516+185_516+186insAA