Canonical Allele Identifier: CA2648419609

Gene: NAXE

Linked Data

• gnomAD v4: 1-156592848-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592848_156592849insA , CM000663.2:g.156592848_156592849insA	GRCh38
NC_000001.10:g.156562640_156562641insA , CM000663.1:g.156562640_156562641insA	GRCh37
NC_000001.9:g.154829264_154829265insA	NCBI36
NG_052542.1:g.6083_6084insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.516+178_516+179insA MANE Select	ENSP00000357218.3:n.516+178_516+179insA
ENST00000467374.2:n.804_805insA
ENST00000679369.1:c.405+178_405+179insA	ENSP00000505883.1:n.405+178_405+179insA
ENST00000679649.1:n.555+178_555+179insA
ENST00000679702.1:c.516+178_516+179insA	ENSP00000505913.1:n.516+178_516+179insA
ENST00000679913.1:n.720+178_720+179insA
ENST00000680004.1:c.516+178_516+179insA	ENSP00000506275.1:n.516+178_516+179insA
ENST00000680087.1:c.516+178_516+179insA	ENSP00000505907.1:n.516+178_516+179insA
ENST00000680269.1:c.516+178_516+179insA	ENSP00000505899.1:n.516+178_516+179insA
ENST00000680529.1:n.700+178_700+179insA
ENST00000680661.1:c.516+178_516+179insA	ENSP00000505088.1:n.516+178_516+179insA
ENST00000681054.1:c.516+178_516+179insA	ENSP00000506192.1:n.516+178_516+179insA
ENST00000681523.1:c.516+178_516+179insA	ENSP00000505349.1:n.516+178_516+179insA
ENST00000681645.1:n.555+178_555+179insA
ENST00000681734.1:c.516+178_516+179insA	ENSP00000506177.1:n.516+178_516+179insA
ENST00000681825.1:n.498_499insA
ENST00000681922.1:n.733_734insA
ENST00000368233.3:c.516+178_516+179insA	ENSP00000357216.3:n.516+178_516+179insA
ENST00000368234.7:c.516+178_516+179insA	ENSP00000357217.3:n.516+178_516+179insA
ENST00000368235.7:c.516+178_516+179insA	ENSP00000357218.3:n.516+178_516+179insA
ENST00000467374.1:n.603_604insA
NM_144772.2:c.516+178_516+179insA	NP_658985.2:n.516+178_516+179insA
XM_017000319.2:c.516+178_516+179insA	XP_016855808.1:n.516+178_516+179insA
NM_144772.3:c.516+178_516+179insA MANE Select	NP_658985.2:n.516+178_516+179insA