Canonical Allele Identifier: CA2646275845

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942929-CCTGGAACTTTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942932_77942943del , CM000663.2:g.77942932_77942943del	GRCh38
NC_000001.10:g.78408617_78408628del , CM000663.1:g.78408617_78408628del	GRCh37
NC_000001.9:g.78181205_78181216del	NCBI36
NG_016625.1:g.59418_59429del , LRG_442:g.59418_59429del
NG_033243.2:g.41153_41164del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*103_*114del MANE Select	ENSP00000333938.7:n.*103_*114del
ENST00000330010.12:c.*103_*114del	ENSP00000327363.8:n.*103_*114del
ENST00000334785.11:c.*103_*114del	ENSP00000333938.7:n.*103_*114del
ENST00000342754.5:c.1749_1760del
ENST00000480732.2:n.1705_1716del
NM_001172309.1:c.*103_*114del	NP_001165780.1:n.*103_*114del
NM_144573.3:c.*103_*114del , LRG_442t1:c.*103_*114del	NP_653174.3:n.*103_*114del
XM_005271322.2:c.*19_*30del	XP_005271379.1:n.*19_*30del
XM_005271323.2:c.*19_*30del	XP_005271380.1:n.*19_*30del
XM_005271324.3:c.*19_*30del	XP_005271381.1:n.*19_*30del
XM_005271325.2:c.*19_*30del	XP_005271382.1:n.*19_*30del
XM_005271326.2:c.*19_*30del	XP_005271383.1:n.*19_*30del
XM_005271327.2:c.*19_*30del	XP_005271384.1:n.*19_*30del
XM_005271322.4:c.*19_*30del	XP_005271379.1:n.*19_*30del
XM_005271323.4:c.*19_*30del	XP_005271380.1:n.*19_*30del
XM_005271324.5:c.*19_*30del	XP_005271381.1:n.*19_*30del
XM_005271325.4:c.*19_*30del	XP_005271382.1:n.*19_*30del
XM_005271326.4:c.*19_*30del	XP_005271383.1:n.*19_*30del
XM_005271327.4:c.*19_*30del	XP_005271384.1:n.*19_*30del
NM_001172309.2:c.*103_*114del	NP_001165780.1:n.*103_*114del
NM_144573.4:c.*103_*114del MANE Select	NP_653174.3:n.*103_*114del