Canonical Allele Identifier: CA1008098221

Gene: NAXE

Linked Data

• dbSNP Id: rs1677363391
• gnomAD v3: 1-156592620-A-ACAT
• gnomAD v4: 1-156592620-A-ACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592621_156592622insATC , CM000663.2:g.156592621_156592622insATC	GRCh38
NC_000001.10:g.156562413_156562414insATC , CM000663.1:g.156562413_156562414insATC	GRCh37
NC_000001.9:g.154829037_154829038insATC	NCBI36
NG_052542.1:g.5856_5857insATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.467_468insATC MANE Select	ENSP00000357218.3:p.Thr156_Gln157insSer
ENST00000467374.2:n.577_578insATC
ENST00000679369.1:c.356_357insATC	ENSP00000505883.1:p.Thr119_Gln120insSer
ENST00000679649.1:n.506_507insATC
ENST00000679702.1:c.467_468insATC	ENSP00000505913.1:p.Thr156_Gln157insSer
ENST00000679913.1:n.671_672insATC
ENST00000680004.1:c.467_468insATC	ENSP00000506275.1:p.Thr156_Gln157insSer
ENST00000680087.1:c.467_468insATC	ENSP00000505907.1:p.Thr156_Gln157insSer
ENST00000680269.1:c.467_468insATC	ENSP00000505899.1:p.Thr156_Gln157insSer
ENST00000680529.1:n.651_652insATC
ENST00000680661.1:c.467_468insATC	ENSP00000505088.1:p.Thr156_Gln157insSer
ENST00000681054.1:c.467_468insATC	ENSP00000506192.1:p.Thr156_Gln157insSer
ENST00000681523.1:c.467_468insATC	ENSP00000505349.1:p.Thr156_Gln157insSer
ENST00000681645.1:n.506_507insATC
ENST00000681734.1:c.467_468insATC	ENSP00000506177.1:p.Thr156_Gln157insSer
ENST00000681825.1:n.271_272insATC
ENST00000681922.1:n.506_507insATC
ENST00000368233.3:c.467_468insATC	ENSP00000357216.3:p.Thr156_Gln157insSer
ENST00000368234.7:c.467_468insATC	ENSP00000357217.3:p.Thr156_Gln157insSer
ENST00000368235.7:c.467_468insATC	ENSP00000357218.3:p.Thr156_Gln157insSer
ENST00000467374.1:n.376_377insATC
NM_144772.2:c.467_468insATC	NP_658985.2:p.Thr156_Gln157insSer
XM_017000319.2:c.467_468insATC	XP_016855808.1:p.Thr156_Gln157insSer
NM_144772.3:c.467_468insATC MANE Select	NP_658985.2:p.Thr156_Gln157insSer