Canonical Allele Identifier: CA421262718

Gene: NAXE

Linked Data

• MyVariant Identifiers: chr1:g.156562363C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592571C>A , CM000663.2:g.156592571C>A	GRCh38
NC_000001.10:g.156562363C>A , CM000663.1:g.156562363C>A	GRCh37
NC_000001.9:g.154828987C>A	NCBI36
NG_052542.1:g.5806C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.417C>A MANE Select	ENSP00000357218.3:p.Thr139=
ENST00000467374.2:n.527C>A
ENST00000679369.1:c.306C>A	ENSP00000505883.1:p.Thr102=
ENST00000679649.1:n.456C>A
ENST00000679702.1:c.417C>A	ENSP00000505913.1:p.Thr139=
ENST00000679913.1:n.621C>A
ENST00000680004.1:c.417C>A	ENSP00000506275.1:p.Thr139=
ENST00000680087.1:c.417C>A	ENSP00000505907.1:p.Thr139=
ENST00000680269.1:c.417C>A	ENSP00000505899.1:p.Thr139=
ENST00000680529.1:n.601C>A
ENST00000680661.1:c.417C>A	ENSP00000505088.1:p.Thr139=
ENST00000681054.1:c.417C>A	ENSP00000506192.1:p.Thr139=
ENST00000681523.1:c.417C>A	ENSP00000505349.1:p.Thr139=
ENST00000681645.1:n.456C>A
ENST00000681734.1:c.417C>A	ENSP00000506177.1:p.Thr139=
ENST00000681825.1:n.221C>A
ENST00000681922.1:n.456C>A
ENST00000368233.3:c.417C>A	ENSP00000357216.3:p.Thr139=
ENST00000368234.7:c.417C>A	ENSP00000357217.3:p.Thr139=
ENST00000368235.7:c.417C>A	ENSP00000357218.3:p.Thr139=
ENST00000467374.1:n.326C>A
NM_144772.2:c.417C>A	NP_658985.2:p.Thr139=
XM_017000319.2:c.417C>A	XP_016855808.1:p.Thr139=
NM_144772.3:c.417C>A MANE Select	NP_658985.2:p.Thr139=