Canonical Allele Identifier: CA421262741

Gene: NAXE

Linked Data

• gnomAD v4: 1-156592610-T-G
• MyVariant Identifiers: chr1:g.156562402T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592610T>G , CM000663.2:g.156592610T>G	GRCh38
NC_000001.10:g.156562402T>G , CM000663.1:g.156562402T>G	GRCh37
NC_000001.9:g.154829026T>G	NCBI36
NG_052542.1:g.5845T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.456T>G MANE Select	ENSP00000357218.3:p.Thr152=
ENST00000467374.2:n.566T>G
ENST00000679369.1:c.345T>G	ENSP00000505883.1:p.Thr115=
ENST00000679649.1:n.495T>G
ENST00000679702.1:c.456T>G	ENSP00000505913.1:p.Thr152=
ENST00000679913.1:n.660T>G
ENST00000680004.1:c.456T>G	ENSP00000506275.1:p.Thr152=
ENST00000680087.1:c.456T>G	ENSP00000505907.1:p.Thr152=
ENST00000680269.1:c.456T>G	ENSP00000505899.1:p.Thr152=
ENST00000680529.1:n.640T>G
ENST00000680661.1:c.456T>G	ENSP00000505088.1:p.Thr152=
ENST00000681054.1:c.456T>G	ENSP00000506192.1:p.Thr152=
ENST00000681523.1:c.456T>G	ENSP00000505349.1:p.Thr152=
ENST00000681645.1:n.495T>G
ENST00000681734.1:c.456T>G	ENSP00000506177.1:p.Thr152=
ENST00000681825.1:n.260T>G
ENST00000681922.1:n.495T>G
ENST00000368233.3:c.456T>G	ENSP00000357216.3:p.Thr152=
ENST00000368234.7:c.456T>G	ENSP00000357217.3:p.Thr152=
ENST00000368235.7:c.456T>G	ENSP00000357218.3:p.Thr152=
ENST00000467374.1:n.365T>G
NM_144772.2:c.456T>G	NP_658985.2:p.Thr152=
XM_017000319.2:c.456T>G	XP_016855808.1:p.Thr152=
NM_144772.3:c.456T>G MANE Select	NP_658985.2:p.Thr152=