Canonical Allele Identifier: CA1143713865

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935971T= , CM000663.2:g.77935971T=	GRCh38
NC_000001.10:g.78401656T= , CM000663.1:g.78401656T=	GRCh37
NC_000001.9:g.78174244T=	NCBI36
NG_016625.1:g.52457T= , LRG_442:g.52457T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1400T= MANE Select	ENSP00000333938.7:p.Ile467=
ENST00000330010.12:c.1208T=	ENSP00000327363.8:p.Ile403=
ENST00000334785.11:c.1400T=	ENSP00000333938.7:p.Ile467=
ENST00000342754.5:c.1099T=
ENST00000480732.2:n.974T=
NM_001172309.1:c.1208T=	NP_001165780.1:p.Ile403=
NM_144573.3:c.1400T= , LRG_442t1:c.1400T=	NP_653174.3:p.Ile467=
XM_005271322.2:c.1400T=	XP_005271379.1:p.Ile467=
XM_005271323.2:c.1358T=	XP_005271380.1:p.Ile453=
XM_005271324.3:c.1208T=	XP_005271381.1:p.Ile403=
XM_005271325.2:c.1251+2492T=	XP_005271382.1:n.1251+2492T=
XM_005271326.2:c.1166T=	XP_005271383.1:p.Ile389=
XM_005271327.2:c.983T=	XP_005271384.1:p.Ile328=
XM_005271322.4:c.1400T=	XP_005271379.1:p.Ile467=
XM_005271323.4:c.1358T=	XP_005271380.1:p.Ile453=
XM_005271324.5:c.1208T=	XP_005271381.1:p.Ile403=
XM_005271325.4:c.1251+2492T=	XP_005271382.1:n.1251+2492T=
XM_005271326.4:c.1166T=	XP_005271383.1:p.Ile389=
XM_005271327.4:c.983T=	XP_005271384.1:p.Ile328=
NM_001172309.2:c.1208T=	NP_001165780.1:p.Ile403=
NM_144573.4:c.1400T= MANE Select	NP_653174.3:p.Ile467=