Canonical Allele Identifier: CA1140265193

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943108G= , CM000663.2:g.77943108G=	GRCh38
NC_000001.10:g.78408793G= , CM000663.1:g.78408793G=	GRCh37
NC_000001.9:g.78181381G=	NCBI36
NG_016625.1:g.59594G= , LRG_442:g.59594G=
NG_033243.2:g.40986C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*279G= MANE Select	ENSP00000333938.7:n.*279G=
ENST00000330010.12:c.*279G=	ENSP00000327363.8:n.*279G=
ENST00000334785.11:c.*279G=	ENSP00000333938.7:n.*279G=
ENST00000342754.5:c.1925G=
ENST00000480732.2:n.1881G=
NM_001172309.1:c.*279G=	NP_001165780.1:n.*279G=
NM_144573.3:c.*279G= , LRG_442t1:c.*279G=	NP_653174.3:n.*279G=
XM_005271322.2:c.*195G=	XP_005271379.1:n.*195G=
XM_005271323.2:c.*195G=	XP_005271380.1:n.*195G=
XM_005271324.3:c.*195G=	XP_005271381.1:n.*195G=
XM_005271325.2:c.*195G=	XP_005271382.1:n.*195G=
XM_005271326.2:c.*195G=	XP_005271383.1:n.*195G=
XM_005271327.2:c.*195G=	XP_005271384.1:n.*195G=
XM_005271322.4:c.*195G=	XP_005271379.1:n.*195G=
XM_005271323.4:c.*195G=	XP_005271380.1:n.*195G=
XM_005271324.5:c.*195G=	XP_005271381.1:n.*195G=
XM_005271325.4:c.*195G=	XP_005271382.1:n.*195G=
XM_005271326.4:c.*195G=	XP_005271383.1:n.*195G=
XM_005271327.4:c.*195G=	XP_005271384.1:n.*195G=
NM_001172309.2:c.*279G=	NP_001165780.1:n.*279G=
NM_144573.4:c.*279G= MANE Select	NP_653174.3:n.*279G=