Canonical Allele Identifier: CA739054669

Gene: NEXN

Linked Data

• dbSNP Id: rs200823109
• gnomAD v3: 1-77935659-CTT-C
• gnomAD v4: 1-77935659-CTT-C
• MyVariant Identifiers: chr1:g.78401345_78401346del (hg19) ; chr1:g.77935660_77935661del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935668_77935669del , CM000663.2:g.77935668_77935669del	GRCh38
NC_000001.10:g.78401353_78401354del , CM000663.1:g.78401353_78401354del	GRCh37
NC_000001.9:g.78173941_78173942del	NCBI36
NG_016625.1:g.52154_52155del , LRG_442:g.52154_52155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-155_1252-154del MANE Select	ENSP00000333938.7:n.1252-155_1252-154del
ENST00000330010.12:c.1060-155_1060-154del	ENSP00000327363.8:n.1060-155_1060-154del
ENST00000334785.11:c.1252-155_1252-154del	ENSP00000333938.7:n.1252-155_1252-154del
ENST00000342754.5:c.951-155_951-154del
ENST00000440324.5:c.1210-155_1210-154del	ENSP00000411902.1:n.1210-155_1210-154del
ENST00000464998.1:n.712-155_712-154del
ENST00000480732.2:n.826-155_826-154del
NM_001172309.1:c.1060-155_1060-154del	NP_001165780.1:n.1060-155_1060-154del
NM_144573.3:c.1252-155_1252-154del , LRG_442t1:c.1252-155_1252-154del	NP_653174.3:n.1252-155_1252-154del
XM_005271322.2:c.1252-155_1252-154del	XP_005271379.1:n.1252-155_1252-154del
XM_005271323.2:c.1210-155_1210-154del	XP_005271380.1:n.1210-155_1210-154del
XM_005271324.3:c.1060-155_1060-154del	XP_005271381.1:n.1060-155_1060-154del
XM_005271325.2:c.1251+2189_1251+2190del	XP_005271382.1:n.1251+2189_1251+2190del
XM_005271326.2:c.1018-155_1018-154del	XP_005271383.1:n.1018-155_1018-154del
XM_005271327.2:c.835-155_835-154del	XP_005271384.1:n.835-155_835-154del
XM_005271322.4:c.1252-155_1252-154del	XP_005271379.1:n.1252-155_1252-154del
XM_005271323.4:c.1210-155_1210-154del	XP_005271380.1:n.1210-155_1210-154del
XM_005271324.5:c.1060-155_1060-154del	XP_005271381.1:n.1060-155_1060-154del
XM_005271325.4:c.1251+2189_1251+2190del	XP_005271382.1:n.1251+2189_1251+2190del
XM_005271326.4:c.1018-155_1018-154del	XP_005271383.1:n.1018-155_1018-154del
XM_005271327.4:c.835-155_835-154del	XP_005271384.1:n.835-155_835-154del
NM_001172309.2:c.1060-155_1060-154del	NP_001165780.1:n.1060-155_1060-154del
NM_144573.4:c.1252-155_1252-154del MANE Select	NP_653174.3:n.1252-155_1252-154del