Canonical Allele Identifier: CA1162778
Gene: NAXE HGNC NCBI

Linked Data

dbSNP Id: rs753953377

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156592595C>A , CM000663.2:g.156592595C>A GRCh38
NC_000001.10:g.156562387C>A , CM000663.1:g.156562387C>A GRCh37
NC_000001.9:g.154829011C>A NCBI36
NG_052542.1:g.5830C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368235.8:c.441C>A MANE Select ENSP00000357218.3:p.Asn147Lys
ENST00000467374.2:n.551C>A
ENST00000679369.1:c.330C>A ENSP00000505883.1:p.Asn110Lys
ENST00000679649.1:n.480C>A
ENST00000679702.1:c.441C>A ENSP00000505913.1:p.Asn147Lys
ENST00000679913.1:n.645C>A
ENST00000680004.1:c.441C>A ENSP00000506275.1:p.Asn147Lys
ENST00000680087.1:c.441C>A ENSP00000505907.1:p.Asn147Lys
ENST00000680269.1:c.441C>A ENSP00000505899.1:p.Asn147Lys
ENST00000680529.1:n.625C>A
ENST00000680661.1:c.441C>A ENSP00000505088.1:p.Asn147Lys
ENST00000681054.1:c.441C>A ENSP00000506192.1:p.Asn147Lys
ENST00000681523.1:c.441C>A ENSP00000505349.1:p.Asn147Lys
ENST00000681645.1:n.480C>A
ENST00000681734.1:c.441C>A ENSP00000506177.1:p.Asn147Lys
ENST00000681825.1:n.245C>A
ENST00000681922.1:n.480C>A
ENST00000368233.3:c.441C>A ENSP00000357216.3:p.Asn147Lys
ENST00000368234.7:c.441C>A ENSP00000357217.3:p.Asn147Lys
ENST00000368235.7:c.441C>A ENSP00000357218.3:p.Asn147Lys
ENST00000467374.1:n.350C>A
NM_144772.2:c.441C>A NP_658985.2:p.Asn147Lys
XM_017000319.2:c.441C>A XP_016855808.1:p.Asn147Lys
NM_144772.3:c.441C>A MANE Select NP_658985.2:p.Asn147Lys