Canonical Allele Identifier: CA1003483095

Gene: NEXN

Linked Data

• dbSNP Id: rs1650751876
• gnomAD v3: 1-77936199-T-TA
• gnomAD v4: 1-77936199-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936200dup , CM000663.2:g.77936200dup	GRCh38
NC_000001.10:g.78401885dup , CM000663.1:g.78401885dup	GRCh37
NC_000001.9:g.78174473dup	NCBI36
NG_016625.1:g.52686dup , LRG_442:g.52686dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+156dup MANE Select	ENSP00000333938.7:n.1473+156dup
ENST00000330010.12:c.1281+156dup	ENSP00000327363.8:n.1281+156dup
ENST00000334785.11:c.1473+156dup	ENSP00000333938.7:n.1473+156dup
ENST00000342754.5:c.1172+156dup
ENST00000480732.2:n.1047+156dup
NM_001172309.1:c.1281+156dup	NP_001165780.1:n.1281+156dup
NM_144573.3:c.1473+156dup , LRG_442t1:c.1473+156dup	NP_653174.3:n.1473+156dup
XM_005271322.2:c.1473+156dup	XP_005271379.1:n.1473+156dup
XM_005271323.2:c.1431+156dup	XP_005271380.1:n.1431+156dup
XM_005271324.3:c.1281+156dup	XP_005271381.1:n.1281+156dup
XM_005271325.2:c.1251+2721dup	XP_005271382.1:n.1251+2721dup
XM_005271326.2:c.1239+156dup	XP_005271383.1:n.1239+156dup
XM_005271327.2:c.1056+156dup	XP_005271384.1:n.1056+156dup
XM_005271322.4:c.1473+156dup	XP_005271379.1:n.1473+156dup
XM_005271323.4:c.1431+156dup	XP_005271380.1:n.1431+156dup
XM_005271324.5:c.1281+156dup	XP_005271381.1:n.1281+156dup
XM_005271325.4:c.1251+2721dup	XP_005271382.1:n.1251+2721dup
XM_005271326.4:c.1239+156dup	XP_005271383.1:n.1239+156dup
XM_005271327.4:c.1056+156dup	XP_005271384.1:n.1056+156dup
NM_001172309.2:c.1281+156dup	NP_001165780.1:n.1281+156dup
NM_144573.4:c.1473+156dup MANE Select	NP_653174.3:n.1473+156dup