Canonical Allele Identifier: CA1177626091

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942823G= , CM000663.2:g.77942823G=	GRCh38
NC_000001.10:g.78408508G= , CM000663.1:g.78408508G=	GRCh37
NC_000001.9:g.78181096G=	NCBI36
NG_016625.1:g.59309G= , LRG_442:g.59309G=
NG_033243.2:g.41271C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.2022G= MANE Select	ENSP00000333938.7:p.Lys674=
ENST00000330010.12:c.1830G=	ENSP00000327363.8:p.Lys610=
ENST00000334785.11:c.2022G=	ENSP00000333938.7:p.Lys674=
ENST00000342754.5:c.1716+5G=
ENST00000480732.2:n.1596G=
NM_001172309.1:c.1830G=	NP_001165780.1:p.Lys610=
NM_144573.3:c.2022G= , LRG_442t1:c.2022G=	NP_653174.3:p.Lys674=
XM_005271322.2:c.2017+5G=	XP_005271379.1:n.2017+5G=
XM_005271323.2:c.1975+5G=	XP_005271380.1:n.1975+5G=
XM_005271324.3:c.1825+5G=	XP_005271381.1:n.1825+5G=
XM_005271325.2:c.1795+5G=	XP_005271382.1:n.1795+5G=
XM_005271326.2:c.1783+5G=	XP_005271383.1:n.1783+5G=
XM_005271327.2:c.1600+5G=	XP_005271384.1:n.1600+5G=
XM_005271322.4:c.2017+5G=	XP_005271379.1:n.2017+5G=
XM_005271323.4:c.1975+5G=	XP_005271380.1:n.1975+5G=
XM_005271324.5:c.1825+5G=	XP_005271381.1:n.1825+5G=
XM_005271325.4:c.1795+5G=	XP_005271382.1:n.1795+5G=
XM_005271326.4:c.1783+5G=	XP_005271383.1:n.1783+5G=
XM_005271327.4:c.1600+5G=	XP_005271384.1:n.1600+5G=
NM_001172309.2:c.1830G=	NP_001165780.1:p.Lys610=
NM_144573.4:c.2022G= MANE Select	NP_653174.3:p.Lys674=