Canonical Allele Identifier: CA2646301246

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942980-TGGCGGGGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942981_77942989del , CM000663.2:g.77942981_77942989del	GRCh38
NC_000001.10:g.78408666_78408674del , CM000663.1:g.78408666_78408674del	GRCh37
NC_000001.9:g.78181254_78181262del	NCBI36
NG_016625.1:g.59467_59475del , LRG_442:g.59467_59475del
NG_033243.2:g.41105_41113del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*152_*160del MANE Select	ENSP00000333938.7:n.*152_*160del
ENST00000330010.12:c.*152_*160del	ENSP00000327363.8:n.*152_*160del
ENST00000334785.11:c.*152_*160del	ENSP00000333938.7:n.*152_*160del
ENST00000342754.5:c.1798_1806del
ENST00000480732.2:n.1754_1762del
NM_001172309.1:c.*152_*160del	NP_001165780.1:n.*152_*160del
NM_144573.3:c.*152_*160del , LRG_442t1:c.*152_*160del	NP_653174.3:n.*152_*160del
XM_005271322.2:c.*68_*76del	XP_005271379.1:n.*68_*76del
XM_005271323.2:c.*68_*76del	XP_005271380.1:n.*68_*76del
XM_005271324.3:c.*68_*76del	XP_005271381.1:n.*68_*76del
XM_005271325.2:c.*68_*76del	XP_005271382.1:n.*68_*76del
XM_005271326.2:c.*68_*76del	XP_005271383.1:n.*68_*76del
XM_005271327.2:c.*68_*76del	XP_005271384.1:n.*68_*76del
XM_005271322.4:c.*68_*76del	XP_005271379.1:n.*68_*76del
XM_005271323.4:c.*68_*76del	XP_005271380.1:n.*68_*76del
XM_005271324.5:c.*68_*76del	XP_005271381.1:n.*68_*76del
XM_005271325.4:c.*68_*76del	XP_005271382.1:n.*68_*76del
XM_005271326.4:c.*68_*76del	XP_005271383.1:n.*68_*76del
XM_005271327.4:c.*68_*76del	XP_005271384.1:n.*68_*76del
NM_001172309.2:c.*152_*160del	NP_001165780.1:n.*152_*160del
NM_144573.4:c.*152_*160del MANE Select	NP_653174.3:n.*152_*160del