Canonical Allele Identifier: CA1200667011

Gene: NAXE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592602C= , CM000663.2:g.156592602C=	GRCh38
NC_000001.10:g.156562394C= , CM000663.1:g.156562394C=	GRCh37
NC_000001.9:g.154829018C=	NCBI36
NG_052542.1:g.5837C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.448C= MANE Select	ENSP00000357218.3:p.Leu150=
ENST00000467374.2:n.558C=
ENST00000679369.1:c.337C=	ENSP00000505883.1:p.Leu113=
ENST00000679649.1:n.487C=
ENST00000679702.1:c.448C=	ENSP00000505913.1:p.Leu150=
ENST00000679913.1:n.652C=
ENST00000680004.1:c.448C=	ENSP00000506275.1:p.Leu150=
ENST00000680087.1:c.448C=	ENSP00000505907.1:p.Leu150=
ENST00000680269.1:c.448C=	ENSP00000505899.1:p.Leu150=
ENST00000680529.1:n.632C=
ENST00000680661.1:c.448C=	ENSP00000505088.1:p.Leu150=
ENST00000681054.1:c.448C=	ENSP00000506192.1:p.Leu150=
ENST00000681523.1:c.448C=	ENSP00000505349.1:p.Leu150=
ENST00000681645.1:n.487C=
ENST00000681734.1:c.448C=	ENSP00000506177.1:p.Leu150=
ENST00000681825.1:n.252C=
ENST00000681922.1:n.487C=
ENST00000368233.3:c.448C=	ENSP00000357216.3:p.Leu150=
ENST00000368234.7:c.448C=	ENSP00000357217.3:p.Leu150=
ENST00000368235.7:c.448C=	ENSP00000357218.3:p.Leu150=
ENST00000467374.1:n.357C=
NM_144772.2:c.448C=	NP_658985.2:p.Leu150=
XM_017000319.2:c.448C=	XP_016855808.1:p.Leu150=
NM_144772.3:c.448C= MANE Select	NP_658985.2:p.Leu150=