Canonical Allele Identifier: CA24692474

Gene: NEXN

Linked Data

• dbSNP Id: rs555129188
• gnomAD v3: 1-77943040-AAC-A
• gnomAD v4: 1-77943040-AAC-A
• MyVariant Identifiers: chr1:g.78408726_78408727del (hg19) ; chr1:g.77943041_77943042del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943042_77943043del , CM000663.2:g.77943042_77943043del	GRCh38
NC_000001.10:g.78408727_78408728del , CM000663.1:g.78408727_78408728del	GRCh37
NC_000001.9:g.78181315_78181316del	NCBI36
NG_016625.1:g.59528_59529del , LRG_442:g.59528_59529del
NG_033243.2:g.41052_41053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*213_*214del MANE Select	ENSP00000333938.7:n.*213_*214del
ENST00000330010.12:c.*213_*214del	ENSP00000327363.8:n.*213_*214del
ENST00000334785.11:c.*213_*214del	ENSP00000333938.7:n.*213_*214del
ENST00000342754.5:c.1859_1860del
ENST00000480732.2:n.1815_1816del
NM_001172309.1:c.*213_*214del	NP_001165780.1:n.*213_*214del
NM_144573.3:c.*213_*214del , LRG_442t1:c.*213_*214del	NP_653174.3:n.*213_*214del
XM_005271322.2:c.*129_*130del	XP_005271379.1:n.*129_*130del
XM_005271323.2:c.*129_*130del	XP_005271380.1:n.*129_*130del
XM_005271324.3:c.*129_*130del	XP_005271381.1:n.*129_*130del
XM_005271325.2:c.*129_*130del	XP_005271382.1:n.*129_*130del
XM_005271326.2:c.*129_*130del	XP_005271383.1:n.*129_*130del
XM_005271327.2:c.*129_*130del	XP_005271384.1:n.*129_*130del
XM_005271322.4:c.*129_*130del	XP_005271379.1:n.*129_*130del
XM_005271323.4:c.*129_*130del	XP_005271380.1:n.*129_*130del
XM_005271324.5:c.*129_*130del	XP_005271381.1:n.*129_*130del
XM_005271325.4:c.*129_*130del	XP_005271382.1:n.*129_*130del
XM_005271326.4:c.*129_*130del	XP_005271383.1:n.*129_*130del
XM_005271327.4:c.*129_*130del	XP_005271384.1:n.*129_*130del
NM_001172309.2:c.*213_*214del	NP_001165780.1:n.*213_*214del
NM_144573.4:c.*213_*214del MANE Select	NP_653174.3:n.*213_*214del