Canonical Allele Identifier: CA2648419613
Gene: NAXE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156592849_156592850insTA , CM000663.2:g.156592849_156592850insTA GRCh38
NC_000001.10:g.156562641_156562642insTA , CM000663.1:g.156562641_156562642insTA GRCh37
NC_000001.9:g.154829265_154829266insTA NCBI36
NG_052542.1:g.6084_6085insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368235.8:c.516+179_516+180insTA MANE Select ENSP00000357218.3:n.516+179_516+180insTA
ENST00000467374.2:n.805_806insTA
ENST00000679369.1:c.405+179_405+180insTA ENSP00000505883.1:n.405+179_405+180insTA
ENST00000679649.1:n.555+179_555+180insTA
ENST00000679702.1:c.516+179_516+180insTA ENSP00000505913.1:n.516+179_516+180insTA
ENST00000679913.1:n.720+179_720+180insTA
ENST00000680004.1:c.516+179_516+180insTA ENSP00000506275.1:n.516+179_516+180insTA
ENST00000680087.1:c.516+179_516+180insTA ENSP00000505907.1:n.516+179_516+180insTA
ENST00000680269.1:c.516+179_516+180insTA ENSP00000505899.1:n.516+179_516+180insTA
ENST00000680529.1:n.700+179_700+180insTA
ENST00000680661.1:c.516+179_516+180insTA ENSP00000505088.1:n.516+179_516+180insTA
ENST00000681054.1:c.516+179_516+180insTA ENSP00000506192.1:n.516+179_516+180insTA
ENST00000681523.1:c.516+179_516+180insTA ENSP00000505349.1:n.516+179_516+180insTA
ENST00000681645.1:n.555+179_555+180insTA
ENST00000681734.1:c.516+179_516+180insTA ENSP00000506177.1:n.516+179_516+180insTA
ENST00000681825.1:n.499_500insTA
ENST00000681922.1:n.734_735insTA
ENST00000368233.3:c.516+179_516+180insTA ENSP00000357216.3:n.516+179_516+180insTA
ENST00000368234.7:c.516+179_516+180insTA ENSP00000357217.3:n.516+179_516+180insTA
ENST00000368235.7:c.516+179_516+180insTA ENSP00000357218.3:n.516+179_516+180insTA
ENST00000467374.1:n.604_605insTA
NM_144772.2:c.516+179_516+180insTA NP_658985.2:n.516+179_516+180insTA
XM_017000319.2:c.516+179_516+180insTA XP_016855808.1:n.516+179_516+180insTA
NM_144772.3:c.516+179_516+180insTA MANE Select NP_658985.2:n.516+179_516+180insTA