Canonical Allele Identifier: CA342873598

Gene: NAXE

Linked Data

• gnomAD v4: 1-156592608-A-C
• MyVariant Identifiers: chr1:g.156562400A>C (hg19) ; chr1:g.156592608A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592608A>C , CM000663.2:g.156592608A>C	GRCh38
NC_000001.10:g.156562400A>C , CM000663.1:g.156562400A>C	GRCh37
NC_000001.9:g.154829024A>C	NCBI36
NG_052542.1:g.5843A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.454A>C MANE Select	ENSP00000357218.3:p.Thr152Pro
ENST00000467374.2:n.564A>C
ENST00000679369.1:c.343A>C	ENSP00000505883.1:p.Thr115Pro
ENST00000679649.1:n.493A>C
ENST00000679702.1:c.454A>C	ENSP00000505913.1:p.Thr152Pro
ENST00000679913.1:n.658A>C
ENST00000680004.1:c.454A>C	ENSP00000506275.1:p.Thr152Pro
ENST00000680087.1:c.454A>C	ENSP00000505907.1:p.Thr152Pro
ENST00000680269.1:c.454A>C	ENSP00000505899.1:p.Thr152Pro
ENST00000680529.1:n.638A>C
ENST00000680661.1:c.454A>C	ENSP00000505088.1:p.Thr152Pro
ENST00000681054.1:c.454A>C	ENSP00000506192.1:p.Thr152Pro
ENST00000681523.1:c.454A>C	ENSP00000505349.1:p.Thr152Pro
ENST00000681645.1:n.493A>C
ENST00000681734.1:c.454A>C	ENSP00000506177.1:p.Thr152Pro
ENST00000681825.1:n.258A>C
ENST00000681922.1:n.493A>C
ENST00000368233.3:c.454A>C	ENSP00000357216.3:p.Thr152Pro
ENST00000368234.7:c.454A>C	ENSP00000357217.3:p.Thr152Pro
ENST00000368235.7:c.454A>C	ENSP00000357218.3:p.Thr152Pro
ENST00000467374.1:n.363A>C
NM_144772.2:c.454A>C	NP_658985.2:p.Thr152Pro
XM_017000319.2:c.454A>C	XP_016855808.1:p.Thr152Pro
NM_144772.3:c.454A>C MANE Select	NP_658985.2:p.Thr152Pro