Canonical Allele Identifier: CA2648419727

Gene: NAXE

Linked Data

• gnomAD v4: 1-156592927-TGCCCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592930_156592935del , CM000663.2:g.156592930_156592935del	GRCh38
NC_000001.10:g.156562722_156562727del , CM000663.1:g.156562722_156562727del	GRCh37
NC_000001.9:g.154829346_154829351del	NCBI36
NG_052542.1:g.6165_6170del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.516+260_516+265del MANE Select	ENSP00000357218.3:n.516+260_516+265del
ENST00000467374.2:n.886_891del
ENST00000679369.1:c.405+260_405+265del	ENSP00000505883.1:n.405+260_405+265del
ENST00000679649.1:n.555+260_555+265del
ENST00000679702.1:c.516+260_516+265del	ENSP00000505913.1:n.516+260_516+265del
ENST00000679913.1:n.720+260_720+265del
ENST00000680004.1:c.516+260_516+265del	ENSP00000506275.1:n.516+260_516+265del
ENST00000680087.1:c.516+260_516+265del	ENSP00000505907.1:n.516+260_516+265del
ENST00000680269.1:c.516+260_516+265del	ENSP00000505899.1:n.516+260_516+265del
ENST00000680529.1:n.700+260_700+265del
ENST00000680661.1:c.516+260_516+265del	ENSP00000505088.1:n.516+260_516+265del
ENST00000681054.1:c.516+260_516+265del	ENSP00000506192.1:n.516+260_516+265del
ENST00000681523.1:c.516+260_516+265del	ENSP00000505349.1:n.516+260_516+265del
ENST00000681645.1:n.555+260_555+265del
ENST00000681734.1:c.516+260_516+265del	ENSP00000506177.1:n.516+260_516+265del
ENST00000681825.1:n.580_585del
ENST00000681922.1:n.815_820del
ENST00000368233.3:c.516+260_516+265del	ENSP00000357216.3:n.516+260_516+265del
ENST00000368234.7:c.516+260_516+265del	ENSP00000357217.3:n.516+260_516+265del
ENST00000368235.7:c.516+260_516+265del	ENSP00000357218.3:n.516+260_516+265del
ENST00000467374.1:n.685_690del
NM_144772.2:c.516+260_516+265del	NP_658985.2:n.516+260_516+265del
XM_017000319.2:c.516+260_516+265del	XP_016855808.1:n.516+260_516+265del
NM_144772.3:c.516+260_516+265del MANE Select	NP_658985.2:n.516+260_516+265del