Canonical Allele Identifier: CA2838197172

Gene: NAXE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156594127C>A , CM000663.2:g.156594127C>A	GRCh38
NC_000001.10:g.156563919C>A , CM000663.1:g.156563919C>A	GRCh37
NC_000001.9:g.154830543C>A	NCBI36
NG_052542.1:g.7362C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.*43C>A MANE Select	ENSP00000357218.3:n.*43C>A
ENST00000467374.2:n.2083C>A
ENST00000679369.1:c.553+572C>A	ENSP00000505883.1:n.553+572C>A
ENST00000679649.1:n.949C>A
ENST00000679702.1:c.*6+37C>A	ENSP00000505913.1:n.*6+37C>A
ENST00000679913.1:n.1077+37C>A
ENST00000680004.1:c.*6+37C>A	ENSP00000506275.1:n.*6+37C>A
ENST00000680087.1:c.664+572C>A	ENSP00000505907.1:n.664+572C>A
ENST00000680269.1:c.*6+37C>A	ENSP00000505899.1:n.*6+37C>A
ENST00000680529.1:n.1094C>A
ENST00000680661.1:c.664+572C>A	ENSP00000505088.1:n.664+572C>A
ENST00000681054.1:c.*6+37C>A	ENSP00000506192.1:n.*6+37C>A
ENST00000681523.1:c.*6+37C>A	ENSP00000505349.1:n.*6+37C>A
ENST00000681645.1:n.1275C>A
ENST00000681734.1:c.*6+37C>A	ENSP00000506177.1:n.*6+37C>A
ENST00000681825.1:n.1414+37C>A
ENST00000681922.1:n.1649+37C>A
ENST00000368234.7:c.*71C>A	ENSP00000357217.3:n.*71C>A
ENST00000368235.7:c.*43C>A	ENSP00000357218.3:n.*43C>A
ENST00000488840.1:n.527C>A
NM_144772.2:c.*43C>A	NP_658985.2:n.*43C>A
XM_017000319.2:c.681+555C>A	XP_016855808.1:n.681+555C>A
NM_144772.3:c.*43C>A MANE Select	NP_658985.2:n.*43C>A