Canonical Allele Identifier: CA2739708118

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942903A>T , CM000663.2:g.77942903A>T	GRCh38
NC_000001.10:g.78408588A>T , CM000663.1:g.78408588A>T	GRCh37
NC_000001.9:g.78181176A>T	NCBI36
NG_016625.1:g.59389A>T , LRG_442:g.59389A>T
NG_033243.2:g.41191T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*74A>T MANE Select	ENSP00000333938.7:n.*74A>T
ENST00000330010.12:c.*74A>T	ENSP00000327363.8:n.*74A>T
ENST00000334785.11:c.*74A>T	ENSP00000333938.7:n.*74A>T
ENST00000342754.5:c.1720A>T
ENST00000480732.2:n.1676A>T
NM_001172309.1:c.*74A>T	NP_001165780.1:n.*74A>T
NM_144573.3:c.*74A>T , LRG_442t1:c.*74A>T	NP_653174.3:n.*74A>T
XM_005271322.2:c.2021A>T	XP_005271379.1:p.Asp674Val
XM_005271323.2:c.1979A>T	XP_005271380.1:p.Asp660Val
XM_005271324.3:c.1829A>T	XP_005271381.1:p.Asp610Val
XM_005271325.2:c.1799A>T	XP_005271382.1:p.Asp600Val
XM_005271326.2:c.1787A>T	XP_005271383.1:p.Asp596Val
XM_005271327.2:c.1604A>T	XP_005271384.1:p.Asp535Val
XM_005271322.4:c.2021A>T	XP_005271379.1:p.Asp674Val
XM_005271323.4:c.1979A>T	XP_005271380.1:p.Asp660Val
XM_005271324.5:c.1829A>T	XP_005271381.1:p.Asp610Val
XM_005271325.4:c.1799A>T	XP_005271382.1:p.Asp600Val
XM_005271326.4:c.1787A>T	XP_005271383.1:p.Asp596Val
XM_005271327.4:c.1604A>T	XP_005271384.1:p.Asp535Val
NM_001172309.2:c.*74A>T	NP_001165780.1:n.*74A>T
NM_144573.4:c.*74A>T MANE Select	NP_653174.3:n.*74A>T