Canonical Allele Identifier: CA1143417799

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935842C= , CM000663.2:g.77935842C=	GRCh38
NC_000001.10:g.78401527C= , CM000663.1:g.78401527C=	GRCh37
NC_000001.9:g.78174115C=	NCBI36
NG_016625.1:g.52328C= , LRG_442:g.52328C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1271C= MANE Select	ENSP00000333938.7:p.Thr424=
ENST00000330010.12:c.1079C=	ENSP00000327363.8:p.Thr360=
ENST00000334785.11:c.1271C=	ENSP00000333938.7:p.Thr424=
ENST00000342754.5:c.970C=
ENST00000440324.5:c.1229C=	ENSP00000411902.1:p.Thr410=
ENST00000464998.1:n.731C=
ENST00000480732.2:n.845C=
NM_001172309.1:c.1079C=	NP_001165780.1:p.Thr360=
NM_144573.3:c.1271C= , LRG_442t1:c.1271C=	NP_653174.3:p.Thr424=
XM_005271322.2:c.1271C=	XP_005271379.1:p.Thr424=
XM_005271323.2:c.1229C=	XP_005271380.1:p.Thr410=
XM_005271324.3:c.1079C=	XP_005271381.1:p.Thr360=
XM_005271325.2:c.1251+2363C=	XP_005271382.1:n.1251+2363C=
XM_005271326.2:c.1037C=	XP_005271383.1:p.Thr346=
XM_005271327.2:c.854C=	XP_005271384.1:p.Thr285=
XM_005271322.4:c.1271C=	XP_005271379.1:p.Thr424=
XM_005271323.4:c.1229C=	XP_005271380.1:p.Thr410=
XM_005271324.5:c.1079C=	XP_005271381.1:p.Thr360=
XM_005271325.4:c.1251+2363C=	XP_005271382.1:n.1251+2363C=
XM_005271326.4:c.1037C=	XP_005271383.1:p.Thr346=
XM_005271327.4:c.854C=	XP_005271384.1:p.Thr285=
NM_001172309.2:c.1079C=	NP_001165780.1:p.Thr360=
NM_144573.4:c.1271C= MANE Select	NP_653174.3:p.Thr424=