Canonical Allele Identifier: CA2739708124

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942906A>T , CM000663.2:g.77942906A>T	GRCh38
NC_000001.10:g.78408591A>T , CM000663.1:g.78408591A>T	GRCh37
NC_000001.9:g.78181179A>T	NCBI36
NG_016625.1:g.59392A>T , LRG_442:g.59392A>T
NG_033243.2:g.41188T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*77A>T MANE Select	ENSP00000333938.7:n.*77A>T
ENST00000330010.12:c.*77A>T	ENSP00000327363.8:n.*77A>T
ENST00000334785.11:c.*77A>T	ENSP00000333938.7:n.*77A>T
ENST00000342754.5:c.1723A>T
ENST00000480732.2:n.1679A>T
NM_001172309.1:c.*77A>T	NP_001165780.1:n.*77A>T
NM_144573.3:c.*77A>T , LRG_442t1:c.*77A>T	NP_653174.3:n.*77A>T
XM_005271322.2:c.2024A>T	XP_005271379.1:p.Asp675Val
XM_005271323.2:c.1982A>T	XP_005271380.1:p.Asp661Val
XM_005271324.3:c.1832A>T	XP_005271381.1:p.Asp611Val
XM_005271325.2:c.1802A>T	XP_005271382.1:p.Asp601Val
XM_005271326.2:c.1790A>T	XP_005271383.1:p.Asp597Val
XM_005271327.2:c.1607A>T	XP_005271384.1:p.Asp536Val
XM_005271322.4:c.2024A>T	XP_005271379.1:p.Asp675Val
XM_005271323.4:c.1982A>T	XP_005271380.1:p.Asp661Val
XM_005271324.5:c.1832A>T	XP_005271381.1:p.Asp611Val
XM_005271325.4:c.1802A>T	XP_005271382.1:p.Asp601Val
XM_005271326.4:c.1790A>T	XP_005271383.1:p.Asp597Val
XM_005271327.4:c.1607A>T	XP_005271384.1:p.Asp536Val
NM_001172309.2:c.*77A>T	NP_001165780.1:n.*77A>T
NM_144573.4:c.*77A>T MANE Select	NP_653174.3:n.*77A>T