Canonical Allele Identifier: CA1177626731

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933369T= , CM000663.2:g.77933369T=	GRCh38
NC_000001.10:g.78399054T= , CM000663.1:g.78399054T=	GRCh37
NC_000001.9:g.78171642T=	NCBI36
NG_016625.1:g.49855T= , LRG_442:g.49855T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1141T= MANE Select	ENSP00000333938.7:p.Leu381=
ENST00000330010.12:c.949T=	ENSP00000327363.8:p.Leu317=
ENST00000334785.11:c.1141T=	ENSP00000333938.7:p.Leu381=
ENST00000342754.5:c.840T=
ENST00000401035.7:c.949T=	ENSP00000383814.3:p.Leu317=
ENST00000440324.5:c.1099T=	ENSP00000411902.1:p.Leu367=
ENST00000464998.1:n.601T=
ENST00000480732.2:n.715T=
NM_001172309.1:c.949T=	NP_001165780.1:p.Leu317=
NM_144573.3:c.1141T= , LRG_442t1:c.1141T=	NP_653174.3:p.Leu381=
XM_005271322.2:c.1141T=	XP_005271379.1:p.Leu381=
XM_005271323.2:c.1099T=	XP_005271380.1:p.Leu367=
XM_005271324.3:c.949T=	XP_005271381.1:p.Leu317=
XM_005271325.2:c.1141T=	XP_005271382.1:p.Leu381=
XM_005271326.2:c.907T=	XP_005271383.1:p.Leu303=
XM_005271327.2:c.724T=	XP_005271384.1:p.Leu242=
XM_005271322.4:c.1141T=	XP_005271379.1:p.Leu381=
XM_005271323.4:c.1099T=	XP_005271380.1:p.Leu367=
XM_005271324.5:c.949T=	XP_005271381.1:p.Leu317=
XM_005271325.4:c.1141T=	XP_005271382.1:p.Leu381=
XM_005271326.4:c.907T=	XP_005271383.1:p.Leu303=
XM_005271327.4:c.724T=	XP_005271384.1:p.Leu242=
NM_001172309.2:c.949T=	NP_001165780.1:p.Leu317=
NM_144573.4:c.1141T= MANE Select	NP_653174.3:p.Leu381=