Canonical Allele Identifier: CA340876724

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78399028G>A (hg19) ; chr1:g.77933343G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933343G>A , CM000663.2:g.77933343G>A	GRCh38
NC_000001.10:g.78399028G>A , CM000663.1:g.78399028G>A	GRCh37
NC_000001.9:g.78171616G>A	NCBI36
NG_016625.1:g.49829G>A , LRG_442:g.49829G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1115G>A MANE Select	ENSP00000333938.7:p.Gly372Glu
ENST00000330010.12:c.923G>A	ENSP00000327363.8:p.Gly308Glu
ENST00000334785.11:c.1115G>A	ENSP00000333938.7:p.Gly372Glu
ENST00000342754.5:c.814G>A
ENST00000401035.7:c.923G>A	ENSP00000383814.3:p.Gly308Glu
ENST00000440324.5:c.1073G>A	ENSP00000411902.1:p.Gly358Glu
ENST00000464998.1:n.575G>A
ENST00000480732.2:n.689G>A
NM_001172309.1:c.923G>A	NP_001165780.1:p.Gly308Glu
NM_144573.3:c.1115G>A , LRG_442t1:c.1115G>A	NP_653174.3:p.Gly372Glu
XM_005271322.2:c.1115G>A	XP_005271379.1:p.Gly372Glu
XM_005271323.2:c.1073G>A	XP_005271380.1:p.Gly358Glu
XM_005271324.3:c.923G>A	XP_005271381.1:p.Gly308Glu
XM_005271325.2:c.1115G>A	XP_005271382.1:p.Gly372Glu
XM_005271326.2:c.881G>A	XP_005271383.1:p.Gly294Glu
XM_005271327.2:c.698G>A	XP_005271384.1:p.Gly233Glu
XM_005271322.4:c.1115G>A	XP_005271379.1:p.Gly372Glu
XM_005271323.4:c.1073G>A	XP_005271380.1:p.Gly358Glu
XM_005271324.5:c.923G>A	XP_005271381.1:p.Gly308Glu
XM_005271325.4:c.1115G>A	XP_005271382.1:p.Gly372Glu
XM_005271326.4:c.881G>A	XP_005271383.1:p.Gly294Glu
XM_005271327.4:c.698G>A	XP_005271384.1:p.Gly233Glu
NM_001172309.2:c.923G>A	NP_001165780.1:p.Gly308Glu
NM_144573.4:c.1115G>A MANE Select	NP_653174.3:p.Gly372Glu