Canonical Allele Identifier: CA342873301

Gene: NAXE

Linked Data

• gnomAD v4: 1-156592562-C-A
• MyVariant Identifiers: chr1:g.156562354C>A (hg19) ; chr1:g.156592562C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592562C>A , CM000663.2:g.156592562C>A	GRCh38
NC_000001.10:g.156562354C>A , CM000663.1:g.156562354C>A	GRCh37
NC_000001.9:g.154828978C>A	NCBI36
NG_052542.1:g.5797C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.408C>A MANE Select	ENSP00000357218.3:p.Tyr136Ter
ENST00000467374.2:n.518C>A
ENST00000679369.1:c.297C>A	ENSP00000505883.1:p.Tyr99Ter
ENST00000679649.1:n.447C>A
ENST00000679702.1:c.408C>A	ENSP00000505913.1:p.Tyr136Ter
ENST00000679913.1:n.612C>A
ENST00000680004.1:c.408C>A	ENSP00000506275.1:p.Tyr136Ter
ENST00000680087.1:c.408C>A	ENSP00000505907.1:p.Tyr136Ter
ENST00000680269.1:c.408C>A	ENSP00000505899.1:p.Tyr136Ter
ENST00000680529.1:n.592C>A
ENST00000680661.1:c.408C>A	ENSP00000505088.1:p.Tyr136Ter
ENST00000681054.1:c.408C>A	ENSP00000506192.1:p.Tyr136Ter
ENST00000681523.1:c.408C>A	ENSP00000505349.1:p.Tyr136Ter
ENST00000681645.1:n.447C>A
ENST00000681734.1:c.408C>A	ENSP00000506177.1:p.Tyr136Ter
ENST00000681825.1:n.212C>A
ENST00000681922.1:n.447C>A
ENST00000368233.3:c.408C>A	ENSP00000357216.3:p.Tyr136Ter
ENST00000368234.7:c.408C>A	ENSP00000357217.3:p.Tyr136Ter
ENST00000368235.7:c.408C>A	ENSP00000357218.3:p.Tyr136Ter
ENST00000467374.1:n.317C>A
NM_144772.2:c.408C>A	NP_658985.2:p.Tyr136Ter
XM_017000319.2:c.408C>A	XP_016855808.1:p.Tyr136Ter
NM_144772.3:c.408C>A MANE Select	NP_658985.2:p.Tyr136Ter