Canonical Allele Identifier: CA1145182124

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942820T= , CM000663.2:g.77942820T=	GRCh38
NC_000001.10:g.78408505T= , CM000663.1:g.78408505T=	GRCh37
NC_000001.9:g.78181093T=	NCBI36
NG_016625.1:g.59306T= , LRG_442:g.59306T=
NG_033243.2:g.41274A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.2019T= MANE Select	ENSP00000333938.7:p.Ser673=
ENST00000330010.12:c.1827T=	ENSP00000327363.8:p.Ser609=
ENST00000334785.11:c.2019T=	ENSP00000333938.7:p.Ser673=
ENST00000342754.5:c.1716+2T=
ENST00000480732.2:n.1593T=
NM_001172309.1:c.1827T=	NP_001165780.1:p.Ser609=
NM_144573.3:c.2019T= , LRG_442t1:c.2019T=	NP_653174.3:p.Ser673=
XM_005271322.2:c.2017+2T=	XP_005271379.1:n.2017+2T=
XM_005271323.2:c.1975+2T=	XP_005271380.1:n.1975+2T=
XM_005271324.3:c.1825+2T=	XP_005271381.1:n.1825+2T=
XM_005271325.2:c.1795+2T=	XP_005271382.1:n.1795+2T=
XM_005271326.2:c.1783+2T=	XP_005271383.1:n.1783+2T=
XM_005271327.2:c.1600+2T=	XP_005271384.1:n.1600+2T=
XM_005271322.4:c.2017+2T=	XP_005271379.1:n.2017+2T=
XM_005271323.4:c.1975+2T=	XP_005271380.1:n.1975+2T=
XM_005271324.5:c.1825+2T=	XP_005271381.1:n.1825+2T=
XM_005271325.4:c.1795+2T=	XP_005271382.1:n.1795+2T=
XM_005271326.4:c.1783+2T=	XP_005271383.1:n.1783+2T=
XM_005271327.4:c.1600+2T=	XP_005271384.1:n.1600+2T=
NM_001172309.2:c.1827T=	NP_001165780.1:p.Ser609=
NM_144573.4:c.2019T= MANE Select	NP_653174.3:p.Ser673=