Canonical Allele Identifier: CA1200667014

Gene: NAXE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592618_156592637delinsTGACCCAGTGTCAGAAAATG , CM000663.2:g.156592618_156592637delinsTGACCCAGTGTCAGAAAATG	GRCh38
NC_000001.10:g.156562410_156562429delinsTGACCCAGTGTCAGAAAATG , CM000663.1:g.156562410_156562429delinsTGACCCAGTGTCAGAAAATG	GRCh37
NC_000001.9:g.154829034_154829053delinsTGACCCAGTGTCAGAAAATG	NCBI36
NG_052542.1:g.5853_5872delinsTGACCCAGTGTCAGAAAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.464_483delinsTGACCCAGTGTCAGAAAATG MANE Select	ENSP00000357218.3:p.Val155=
ENST00000467374.2:n.574_593delinsTGACCCAGTGTCAGAAAATG
ENST00000679369.1:c.353_372delinsTGACCCAGTGTCAGAAAATG	ENSP00000505883.1:p.Val118=
ENST00000679649.1:n.503_522delinsTGACCCAGTGTCAGAAAATG
ENST00000679702.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000505913.1:p.Val155=
ENST00000679913.1:n.668_687delinsTGACCCAGTGTCAGAAAATG
ENST00000680004.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000506275.1:p.Val155=
ENST00000680087.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000505907.1:p.Val155=
ENST00000680269.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000505899.1:p.Val155=
ENST00000680529.1:n.648_667delinsTGACCCAGTGTCAGAAAATG
ENST00000680661.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000505088.1:p.Val155=
ENST00000681054.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000506192.1:p.Val155=
ENST00000681523.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000505349.1:p.Val155=
ENST00000681645.1:n.503_522delinsTGACCCAGTGTCAGAAAATG
ENST00000681734.1:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000506177.1:p.Val155=
ENST00000681825.1:n.268_287delinsTGACCCAGTGTCAGAAAATG
ENST00000681922.1:n.503_522delinsTGACCCAGTGTCAGAAAATG
ENST00000368233.3:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000357216.3:p.Val155=
ENST00000368234.7:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000357217.3:p.Val155=
ENST00000368235.7:c.464_483delinsTGACCCAGTGTCAGAAAATG	ENSP00000357218.3:p.Val155=
ENST00000467374.1:n.373_392delinsTGACCCAGTGTCAGAAAATG
NM_144772.2:c.464_483delinsTGACCCAGTGTCAGAAAATG	NP_658985.2:p.Val155=
XM_017000319.2:c.464_483delinsTGACCCAGTGTCAGAAAATG	XP_016855808.1:p.Val155=
NM_144772.3:c.464_483delinsTGACCCAGTGTCAGAAAATG MANE Select	NP_658985.2:p.Val155=