Canonical Allele Identifier: CA340881037

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942107-A-G
• MyVariant Identifiers: chr1:g.78407792A>G (hg19) ; chr1:g.77942107A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942107A>G , CM000663.2:g.77942107A>G	GRCh38
NC_000001.10:g.78407792A>G , CM000663.1:g.78407792A>G	GRCh37
NC_000001.9:g.78180380A>G	NCBI36
NG_016625.1:g.58593A>G , LRG_442:g.58593A>G
NG_033243.2:g.41987T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1558A>G MANE Select	ENSP00000333938.7:p.Met520Val
ENST00000330010.12:c.1366A>G	ENSP00000327363.8:p.Met456Val
ENST00000334785.11:c.1558A>G	ENSP00000333938.7:p.Met520Val
ENST00000342754.5:c.1257A>G
ENST00000470735.1:n.397A>G
ENST00000480732.2:n.1132A>G
NM_001172309.1:c.1366A>G	NP_001165780.1:p.Met456Val
NM_144573.3:c.1558A>G , LRG_442t1:c.1558A>G	NP_653174.3:p.Met520Val
XM_005271322.2:c.1558A>G	XP_005271379.1:p.Met520Val
XM_005271323.2:c.1516A>G	XP_005271380.1:p.Met506Val
XM_005271324.3:c.1366A>G	XP_005271381.1:p.Met456Val
XM_005271325.2:c.1336A>G	XP_005271382.1:p.Met446Val
XM_005271326.2:c.1324A>G	XP_005271383.1:p.Met442Val
XM_005271327.2:c.1141A>G	XP_005271384.1:p.Met381Val
XM_005271322.4:c.1558A>G	XP_005271379.1:p.Met520Val
XM_005271323.4:c.1516A>G	XP_005271380.1:p.Met506Val
XM_005271324.5:c.1366A>G	XP_005271381.1:p.Met456Val
XM_005271325.4:c.1336A>G	XP_005271382.1:p.Met446Val
XM_005271326.4:c.1324A>G	XP_005271383.1:p.Met442Val
XM_005271327.4:c.1141A>G	XP_005271384.1:p.Met381Val
NM_001172309.2:c.1366A>G	NP_001165780.1:p.Met456Val
NM_144573.4:c.1558A>G MANE Select	NP_653174.3:p.Met520Val