Canonical Allele Identifier: CA1177628504

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936335C= , CM000663.2:g.77936335C=	GRCh38
NC_000001.10:g.78402020C= , CM000663.1:g.78402020C=	GRCh37
NC_000001.9:g.78174608C=	NCBI36
NG_016625.1:g.52821C= , LRG_442:g.52821C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+291C= MANE Select	ENSP00000333938.7:n.1473+291C=
ENST00000330010.12:c.1281+291C=	ENSP00000327363.8:n.1281+291C=
ENST00000334785.11:c.1473+291C=	ENSP00000333938.7:n.1473+291C=
ENST00000342754.5:c.1172+291C=
ENST00000480732.2:n.1047+291C=
NM_001172309.1:c.1281+291C=	NP_001165780.1:n.1281+291C=
NM_144573.3:c.1473+291C= , LRG_442t1:c.1473+291C=	NP_653174.3:n.1473+291C=
XM_005271322.2:c.1473+291C=	XP_005271379.1:n.1473+291C=
XM_005271323.2:c.1431+291C=	XP_005271380.1:n.1431+291C=
XM_005271324.3:c.1281+291C=	XP_005271381.1:n.1281+291C=
XM_005271325.2:c.1251+2856C=	XP_005271382.1:n.1251+2856C=
XM_005271326.2:c.1239+291C=	XP_005271383.1:n.1239+291C=
XM_005271327.2:c.1056+291C=	XP_005271384.1:n.1056+291C=
XM_005271322.4:c.1473+291C=	XP_005271379.1:n.1473+291C=
XM_005271323.4:c.1431+291C=	XP_005271380.1:n.1431+291C=
XM_005271324.5:c.1281+291C=	XP_005271381.1:n.1281+291C=
XM_005271325.4:c.1251+2856C=	XP_005271382.1:n.1251+2856C=
XM_005271326.4:c.1239+291C=	XP_005271383.1:n.1239+291C=
XM_005271327.4:c.1056+291C=	XP_005271384.1:n.1056+291C=
NM_001172309.2:c.1281+291C=	NP_001165780.1:n.1281+291C=
NM_144573.4:c.1473+291C= MANE Select	NP_653174.3:n.1473+291C=