Canonical Allele Identifier: CA1177631460

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942744A= , CM000663.2:g.77942744A=	GRCh38
NC_000001.10:g.78408429A= , CM000663.1:g.78408429A=	GRCh37
NC_000001.9:g.78181017A=	NCBI36
NG_016625.1:g.59230A= , LRG_442:g.59230A=
NG_033243.2:g.41350T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1943A= MANE Select	ENSP00000333938.7:p.Asp648=
ENST00000330010.12:c.1751A=	ENSP00000327363.8:p.Asp584=
ENST00000334785.11:c.1943A=	ENSP00000333938.7:p.Asp648=
ENST00000342754.5:c.1642A=
ENST00000470735.1:n.782A=
ENST00000480732.2:n.1517A=
NM_001172309.1:c.1751A=	NP_001165780.1:p.Asp584=
NM_144573.3:c.1943A= , LRG_442t1:c.1943A=	NP_653174.3:p.Asp648=
XM_005271322.2:c.1943A=	XP_005271379.1:p.Asp648=
XM_005271323.2:c.1901A=	XP_005271380.1:p.Asp634=
XM_005271324.3:c.1751A=	XP_005271381.1:p.Asp584=
XM_005271325.2:c.1721A=	XP_005271382.1:p.Asp574=
XM_005271326.2:c.1709A=	XP_005271383.1:p.Asp570=
XM_005271327.2:c.1526A=	XP_005271384.1:p.Asp509=
XM_005271322.4:c.1943A=	XP_005271379.1:p.Asp648=
XM_005271323.4:c.1901A=	XP_005271380.1:p.Asp634=
XM_005271324.5:c.1751A=	XP_005271381.1:p.Asp584=
XM_005271325.4:c.1721A=	XP_005271382.1:p.Asp574=
XM_005271326.4:c.1709A=	XP_005271383.1:p.Asp570=
XM_005271327.4:c.1526A=	XP_005271384.1:p.Asp509=
NM_001172309.2:c.1751A=	NP_001165780.1:p.Asp584=
NM_144573.4:c.1943A= MANE Select	NP_653174.3:p.Asp648=