Canonical Allele Identifier: CA340883256

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942750-G-T
• MyVariant Identifiers: chr1:g.78408435G>T (hg19) ; chr1:g.77942750G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942750G>T , CM000663.2:g.77942750G>T	GRCh38
NC_000001.10:g.78408435G>T , CM000663.1:g.78408435G>T	GRCh37
NC_000001.9:g.78181023G>T	NCBI36
NG_016625.1:g.59236G>T , LRG_442:g.59236G>T
NG_033243.2:g.41344C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1949G>T MANE Select	ENSP00000333938.7:p.Gly650Val
ENST00000330010.12:c.1757G>T	ENSP00000327363.8:p.Gly586Val
ENST00000334785.11:c.1949G>T	ENSP00000333938.7:p.Gly650Val
ENST00000342754.5:c.1648G>T
ENST00000470735.1:n.788G>T
ENST00000480732.2:n.1523G>T
NM_001172309.1:c.1757G>T	NP_001165780.1:p.Gly586Val
NM_144573.3:c.1949G>T , LRG_442t1:c.1949G>T	NP_653174.3:p.Gly650Val
XM_005271322.2:c.1949G>T	XP_005271379.1:p.Gly650Val
XM_005271323.2:c.1907G>T	XP_005271380.1:p.Gly636Val
XM_005271324.3:c.1757G>T	XP_005271381.1:p.Gly586Val
XM_005271325.2:c.1727G>T	XP_005271382.1:p.Gly576Val
XM_005271326.2:c.1715G>T	XP_005271383.1:p.Gly572Val
XM_005271327.2:c.1532G>T	XP_005271384.1:p.Gly511Val
XM_005271322.4:c.1949G>T	XP_005271379.1:p.Gly650Val
XM_005271323.4:c.1907G>T	XP_005271380.1:p.Gly636Val
XM_005271324.5:c.1757G>T	XP_005271381.1:p.Gly586Val
XM_005271325.4:c.1727G>T	XP_005271382.1:p.Gly576Val
XM_005271326.4:c.1715G>T	XP_005271383.1:p.Gly572Val
XM_005271327.4:c.1532G>T	XP_005271384.1:p.Gly511Val
NM_001172309.2:c.1757G>T	NP_001165780.1:p.Gly586Val
NM_144573.4:c.1949G>T MANE Select	NP_653174.3:p.Gly650Val