Canonical Allele Identifier: CA1200667023
Gene: NAXE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156592632A= , CM000663.2:g.156592632A= GRCh38
NC_000001.10:g.156562424A= , CM000663.1:g.156562424A= GRCh37
NC_000001.9:g.154829048A= NCBI36
NG_052542.1:g.5867A=

Transcript Alleles

HGVS Amino-acid change
ENST00000368235.8:c.478A= MANE Select ENSP00000357218.3:p.Lys160=
ENST00000467374.2:n.588A=
ENST00000679369.1:c.367A= ENSP00000505883.1:p.Lys123=
ENST00000679649.1:n.517A=
ENST00000679702.1:c.478A= ENSP00000505913.1:p.Lys160=
ENST00000679913.1:n.682A=
ENST00000680004.1:c.478A= ENSP00000506275.1:p.Lys160=
ENST00000680087.1:c.478A= ENSP00000505907.1:p.Lys160=
ENST00000680269.1:c.478A= ENSP00000505899.1:p.Lys160=
ENST00000680529.1:n.662A=
ENST00000680661.1:c.478A= ENSP00000505088.1:p.Lys160=
ENST00000681054.1:c.478A= ENSP00000506192.1:p.Lys160=
ENST00000681523.1:c.478A= ENSP00000505349.1:p.Lys160=
ENST00000681645.1:n.517A=
ENST00000681734.1:c.478A= ENSP00000506177.1:p.Lys160=
ENST00000681825.1:n.282A=
ENST00000681922.1:n.517A=
ENST00000368233.3:c.478A= ENSP00000357216.3:p.Lys160=
ENST00000368234.7:c.478A= ENSP00000357217.3:p.Lys160=
ENST00000368235.7:c.478A= ENSP00000357218.3:p.Lys160=
ENST00000467374.1:n.387A=
NM_144772.2:c.478A= NP_658985.2:p.Lys160=
XM_017000319.2:c.478A= XP_016855808.1:p.Lys160=
NM_144772.3:c.478A= MANE Select NP_658985.2:p.Lys160=