Canonical Allele Identifier: CA1177631447

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942712C= , CM000663.2:g.77942712C=	GRCh38
NC_000001.10:g.78408397C= , CM000663.1:g.78408397C=	GRCh37
NC_000001.9:g.78180985C=	NCBI36
NG_016625.1:g.59198C= , LRG_442:g.59198C=
NG_033243.2:g.41382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1911C= MANE Select	ENSP00000333938.7:p.Tyr637=
ENST00000330010.12:c.1719C=	ENSP00000327363.8:p.Tyr573=
ENST00000334785.11:c.1911C=	ENSP00000333938.7:p.Tyr637=
ENST00000342754.5:c.1610C=
ENST00000470735.1:n.750C=
ENST00000480732.2:n.1485C=
NM_001172309.1:c.1719C=	NP_001165780.1:p.Tyr573=
NM_144573.3:c.1911C= , LRG_442t1:c.1911C=	NP_653174.3:p.Tyr637=
XM_005271322.2:c.1911C=	XP_005271379.1:p.Tyr637=
XM_005271323.2:c.1869C=	XP_005271380.1:p.Tyr623=
XM_005271324.3:c.1719C=	XP_005271381.1:p.Tyr573=
XM_005271325.2:c.1689C=	XP_005271382.1:p.Tyr563=
XM_005271326.2:c.1677C=	XP_005271383.1:p.Tyr559=
XM_005271327.2:c.1494C=	XP_005271384.1:p.Tyr498=
XM_005271322.4:c.1911C=	XP_005271379.1:p.Tyr637=
XM_005271323.4:c.1869C=	XP_005271380.1:p.Tyr623=
XM_005271324.5:c.1719C=	XP_005271381.1:p.Tyr573=
XM_005271325.4:c.1689C=	XP_005271382.1:p.Tyr563=
XM_005271326.4:c.1677C=	XP_005271383.1:p.Tyr559=
XM_005271327.4:c.1494C=	XP_005271384.1:p.Tyr498=
NM_001172309.2:c.1719C=	NP_001165780.1:p.Tyr573=
NM_144573.4:c.1911C= MANE Select	NP_653174.3:p.Tyr637=