Canonical Allele Identifier: CA1177631209

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942203C= , CM000663.2:g.77942203C=	GRCh38
NC_000001.10:g.78407888C= , CM000663.1:g.78407888C=	GRCh37
NC_000001.9:g.78180476C=	NCBI36
NG_016625.1:g.58689C= , LRG_442:g.58689C=
NG_033243.2:g.41891G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1654C= MANE Select	ENSP00000333938.7:p.Gln552=
ENST00000330010.12:c.1462C=	ENSP00000327363.8:p.Gln488=
ENST00000334785.11:c.1654C=	ENSP00000333938.7:p.Gln552=
ENST00000342754.5:c.1353C=
ENST00000470735.1:n.493C=
ENST00000480732.2:n.1228C=
NM_001172309.1:c.1462C=	NP_001165780.1:p.Gln488=
NM_144573.3:c.1654C= , LRG_442t1:c.1654C=	NP_653174.3:p.Gln552=
XM_005271322.2:c.1654C=	XP_005271379.1:p.Gln552=
XM_005271323.2:c.1612C=	XP_005271380.1:p.Gln538=
XM_005271324.3:c.1462C=	XP_005271381.1:p.Gln488=
XM_005271325.2:c.1432C=	XP_005271382.1:p.Gln478=
XM_005271326.2:c.1420C=	XP_005271383.1:p.Gln474=
XM_005271327.2:c.1237C=	XP_005271384.1:p.Gln413=
XM_005271322.4:c.1654C=	XP_005271379.1:p.Gln552=
XM_005271323.4:c.1612C=	XP_005271380.1:p.Gln538=
XM_005271324.5:c.1462C=	XP_005271381.1:p.Gln488=
XM_005271325.4:c.1432C=	XP_005271382.1:p.Gln478=
XM_005271326.4:c.1420C=	XP_005271383.1:p.Gln474=
XM_005271327.4:c.1237C=	XP_005271384.1:p.Gln413=
NM_001172309.2:c.1462C=	NP_001165780.1:p.Gln488=
NM_144573.4:c.1654C= MANE Select	NP_653174.3:p.Gln552=