Canonical Allele Identifier: CA342873524

Gene: NAXE

Linked Data

• MyVariant Identifiers: chr1:g.156562386A>C (hg19) ; chr1:g.156592594A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592594A>C , CM000663.2:g.156592594A>C	GRCh38
NC_000001.10:g.156562386A>C , CM000663.1:g.156562386A>C	GRCh37
NC_000001.9:g.154829010A>C	NCBI36
NG_052542.1:g.5829A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.440A>C MANE Select	ENSP00000357218.3:p.Asn147Thr
ENST00000467374.2:n.550A>C
ENST00000679369.1:c.329A>C	ENSP00000505883.1:p.Asn110Thr
ENST00000679649.1:n.479A>C
ENST00000679702.1:c.440A>C	ENSP00000505913.1:p.Asn147Thr
ENST00000679913.1:n.644A>C
ENST00000680004.1:c.440A>C	ENSP00000506275.1:p.Asn147Thr
ENST00000680087.1:c.440A>C	ENSP00000505907.1:p.Asn147Thr
ENST00000680269.1:c.440A>C	ENSP00000505899.1:p.Asn147Thr
ENST00000680529.1:n.624A>C
ENST00000680661.1:c.440A>C	ENSP00000505088.1:p.Asn147Thr
ENST00000681054.1:c.440A>C	ENSP00000506192.1:p.Asn147Thr
ENST00000681523.1:c.440A>C	ENSP00000505349.1:p.Asn147Thr
ENST00000681645.1:n.479A>C
ENST00000681734.1:c.440A>C	ENSP00000506177.1:p.Asn147Thr
ENST00000681825.1:n.244A>C
ENST00000681922.1:n.479A>C
ENST00000368233.3:c.440A>C	ENSP00000357216.3:p.Asn147Thr
ENST00000368234.7:c.440A>C	ENSP00000357217.3:p.Asn147Thr
ENST00000368235.7:c.440A>C	ENSP00000357218.3:p.Asn147Thr
ENST00000467374.1:n.349A>C
NM_144772.2:c.440A>C	NP_658985.2:p.Asn147Thr
XM_017000319.2:c.440A>C	XP_016855808.1:p.Asn147Thr
NM_144772.3:c.440A>C MANE Select	NP_658985.2:p.Asn147Thr