Canonical Allele Identifier: CA1144494453

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943038A= , CM000663.2:g.77943038A=	GRCh38
NC_000001.10:g.78408723A= , CM000663.1:g.78408723A=	GRCh37
NC_000001.9:g.78181311A=	NCBI36
NG_016625.1:g.59524A= , LRG_442:g.59524A=
NG_033243.2:g.41056T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*209A= MANE Select	ENSP00000333938.7:n.*209A=
ENST00000330010.12:c.*209A=	ENSP00000327363.8:n.*209A=
ENST00000334785.11:c.*209A=	ENSP00000333938.7:n.*209A=
ENST00000342754.5:c.1855A=
ENST00000480732.2:n.1811A=
NM_001172309.1:c.*209A=	NP_001165780.1:n.*209A=
NM_144573.3:c.*209A= , LRG_442t1:c.*209A=	NP_653174.3:n.*209A=
XM_005271322.2:c.*125A=	XP_005271379.1:n.*125A=
XM_005271323.2:c.*125A=	XP_005271380.1:n.*125A=
XM_005271324.3:c.*125A=	XP_005271381.1:n.*125A=
XM_005271325.2:c.*125A=	XP_005271382.1:n.*125A=
XM_005271326.2:c.*125A=	XP_005271383.1:n.*125A=
XM_005271327.2:c.*125A=	XP_005271384.1:n.*125A=
XM_005271322.4:c.*125A=	XP_005271379.1:n.*125A=
XM_005271323.4:c.*125A=	XP_005271380.1:n.*125A=
XM_005271324.5:c.*125A=	XP_005271381.1:n.*125A=
XM_005271325.4:c.*125A=	XP_005271382.1:n.*125A=
XM_005271326.4:c.*125A=	XP_005271383.1:n.*125A=
XM_005271327.4:c.*125A=	XP_005271384.1:n.*125A=
NM_001172309.2:c.*209A=	NP_001165780.1:n.*209A=
NM_144573.4:c.*209A= MANE Select	NP_653174.3:n.*209A=