Canonical Allele Identifier: CA523842824

Gene: NEXN

Linked Data

• dbSNP Id: rs1180967101
• gnomAD v2: 1-78408623-TTC-T
• gnomAD v4: 1-77942938-TTC-T
• MyVariant Identifiers: chr1:g.78408624_78408625del (hg19) ; chr1:g.77942939_77942940del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942942_77942943del , CM000663.2:g.77942942_77942943del	GRCh38
NC_000001.10:g.78408627_78408628del , CM000663.1:g.78408627_78408628del	GRCh37
NC_000001.9:g.78181215_78181216del	NCBI36
NG_016625.1:g.59428_59429del , LRG_442:g.59428_59429del
NG_033243.2:g.41154_41155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*113_*114del MANE Select	ENSP00000333938.7:n.*113_*114del
ENST00000330010.12:c.*113_*114del	ENSP00000327363.8:n.*113_*114del
ENST00000334785.11:c.*113_*114del	ENSP00000333938.7:n.*113_*114del
ENST00000342754.5:c.1759_1760del
ENST00000480732.2:n.1715_1716del
NM_001172309.1:c.*113_*114del	NP_001165780.1:n.*113_*114del
NM_144573.3:c.*113_*114del , LRG_442t1:c.*113_*114del	NP_653174.3:n.*113_*114del
XM_005271322.2:c.*29_*30del	XP_005271379.1:n.*29_*30del
XM_005271323.2:c.*29_*30del	XP_005271380.1:n.*29_*30del
XM_005271324.3:c.*29_*30del	XP_005271381.1:n.*29_*30del
XM_005271325.2:c.*29_*30del	XP_005271382.1:n.*29_*30del
XM_005271326.2:c.*29_*30del	XP_005271383.1:n.*29_*30del
XM_005271327.2:c.*29_*30del	XP_005271384.1:n.*29_*30del
XM_005271322.4:c.*29_*30del	XP_005271379.1:n.*29_*30del
XM_005271323.4:c.*29_*30del	XP_005271380.1:n.*29_*30del
XM_005271324.5:c.*29_*30del	XP_005271381.1:n.*29_*30del
XM_005271325.4:c.*29_*30del	XP_005271382.1:n.*29_*30del
XM_005271326.4:c.*29_*30del	XP_005271383.1:n.*29_*30del
XM_005271327.4:c.*29_*30del	XP_005271384.1:n.*29_*30del
NM_001172309.2:c.*113_*114del	NP_001165780.1:n.*113_*114del
NM_144573.4:c.*113_*114del MANE Select	NP_653174.3:n.*113_*114del