Canonical Allele Identifier: CA1200667091

Gene: NAXE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592817_156592820delinsTCTC , CM000663.2:g.156592817_156592820delinsTCTC	GRCh38
NC_000001.10:g.156562609_156562612delinsTCTC , CM000663.1:g.156562609_156562612delinsTCTC	GRCh37
NC_000001.9:g.154829233_154829236delinsTCTC	NCBI36
NG_052542.1:g.6052_6055delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.516+147_516+150delinsTCTC MANE Select	ENSP00000357218.3:n.516+147_516+150delinsTCTC
ENST00000467374.2:n.773_776delinsTCTC
ENST00000679369.1:c.405+147_405+150delinsTCTC	ENSP00000505883.1:n.405+147_405+150delinsTCTC
ENST00000679649.1:n.555+147_555+150delinsTCTC
ENST00000679702.1:c.516+147_516+150delinsTCTC	ENSP00000505913.1:n.516+147_516+150delinsTCTC
ENST00000679913.1:n.720+147_720+150delinsTCTC
ENST00000680004.1:c.516+147_516+150delinsTCTC	ENSP00000506275.1:n.516+147_516+150delinsTCTC
ENST00000680087.1:c.516+147_516+150delinsTCTC	ENSP00000505907.1:n.516+147_516+150delinsTCTC
ENST00000680269.1:c.516+147_516+150delinsTCTC	ENSP00000505899.1:n.516+147_516+150delinsTCTC
ENST00000680529.1:n.700+147_700+150delinsTCTC
ENST00000680661.1:c.516+147_516+150delinsTCTC	ENSP00000505088.1:n.516+147_516+150delinsTCTC
ENST00000681054.1:c.516+147_516+150delinsTCTC	ENSP00000506192.1:n.516+147_516+150delinsTCTC
ENST00000681523.1:c.516+147_516+150delinsTCTC	ENSP00000505349.1:n.516+147_516+150delinsTCTC
ENST00000681645.1:n.555+147_555+150delinsTCTC
ENST00000681734.1:c.516+147_516+150delinsTCTC	ENSP00000506177.1:n.516+147_516+150delinsTCTC
ENST00000681825.1:n.467_470delinsTCTC
ENST00000681922.1:n.702_705delinsTCTC
ENST00000368233.3:c.516+147_516+150delinsTCTC	ENSP00000357216.3:n.516+147_516+150delinsTCTC
ENST00000368234.7:c.516+147_516+150delinsTCTC	ENSP00000357217.3:n.516+147_516+150delinsTCTC
ENST00000368235.7:c.516+147_516+150delinsTCTC	ENSP00000357218.3:n.516+147_516+150delinsTCTC
ENST00000467374.1:n.572_575delinsTCTC
NM_144772.2:c.516+147_516+150delinsTCTC	NP_658985.2:n.516+147_516+150delinsTCTC
XM_017000319.2:c.516+147_516+150delinsTCTC	XP_016855808.1:n.516+147_516+150delinsTCTC
NM_144772.3:c.516+147_516+150delinsTCTC MANE Select	NP_658985.2:n.516+147_516+150delinsTCTC