Canonical Allele Identifier: CA2646275758

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942870-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942874dup , CM000663.2:g.77942874dup	GRCh38
NC_000001.10:g.78408559dup , CM000663.1:g.78408559dup	GRCh37
NC_000001.9:g.78181147dup	NCBI36
NG_016625.1:g.59360dup , LRG_442:g.59360dup
NG_033243.2:g.41223dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*45dup MANE Select	ENSP00000333938.7:n.*45dup
ENST00000330010.12:c.*45dup	ENSP00000327363.8:n.*45dup
ENST00000334785.11:c.*45dup	ENSP00000333938.7:n.*45dup
ENST00000342754.5:c.1717-26dup
ENST00000480732.2:n.1647dup
NM_001172309.1:c.*45dup	NP_001165780.1:n.*45dup
NM_144573.3:c.*45dup , LRG_442t1:c.*45dup	NP_653174.3:n.*45dup
XM_005271322.2:c.2018-26dup	XP_005271379.1:n.2018-26dup
XM_005271323.2:c.1976-26dup	XP_005271380.1:n.1976-26dup
XM_005271324.3:c.1826-26dup	XP_005271381.1:n.1826-26dup
XM_005271325.2:c.1796-26dup	XP_005271382.1:n.1796-26dup
XM_005271326.2:c.1784-26dup	XP_005271383.1:n.1784-26dup
XM_005271327.2:c.1601-26dup	XP_005271384.1:n.1601-26dup
XM_005271322.4:c.2018-26dup	XP_005271379.1:n.2018-26dup
XM_005271323.4:c.1976-26dup	XP_005271380.1:n.1976-26dup
XM_005271324.5:c.1826-26dup	XP_005271381.1:n.1826-26dup
XM_005271325.4:c.1796-26dup	XP_005271382.1:n.1796-26dup
XM_005271326.4:c.1784-26dup	XP_005271383.1:n.1784-26dup
XM_005271327.4:c.1601-26dup	XP_005271384.1:n.1601-26dup
NM_001172309.2:c.*45dup	NP_001165780.1:n.*45dup
NM_144573.4:c.*45dup MANE Select	NP_653174.3:n.*45dup