Canonical Allele Identifier: CA1003482999

Gene: NEXN

Linked Data

• dbSNP Id: rs1650731675
• gnomAD v3: 1-77936010-A-AAATTAAAGAGCGAGAAGCTGAAAATTTTCATGAGGTATATTACCTTTATATTTAACAT
• gnomAD v4: 1-77936010-A-AAATTAAAGAGCGAGAAGCTGAAAATTTTCATGAGGTATATTACCTTTATATTTAACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936012_77936069dup , CM000663.2:g.77936012_77936069dup	GRCh38
NC_000001.10:g.78401697_78401754dup , CM000663.1:g.78401697_78401754dup	GRCh37
NC_000001.9:g.78174285_78174342dup	NCBI36
NG_016625.1:g.52498_52555dup , LRG_442:g.52498_52555dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1441_1473+25dup
ENST00000330010.12:c.1249_1281+25dup
ENST00000334785.11:c.1441_1473+25dup
ENST00000342754.5:c.1140_1172+25dup
ENST00000480732.2:n.1015_1047+25dup
NM_001172309.1:c.1249_1281+25dup
NM_144573.3:c.1441_1473+25dup , LRG_442t1:c.1441_1473+25dup
XM_005271322.2:c.1441_1473+25dup
XM_005271323.2:c.1399_1431+25dup
XM_005271324.3:c.1249_1281+25dup
XM_005271325.2:c.1251+2533_1251+2590dup	XP_005271382.1:n.1251+2533_1251+2590dup
XM_005271326.2:c.1207_1239+25dup
XM_005271327.2:c.1024_1056+25dup
XM_005271322.4:c.1441_1473+25dup
XM_005271323.4:c.1399_1431+25dup
XM_005271324.5:c.1249_1281+25dup
XM_005271325.4:c.1251+2533_1251+2590dup	XP_005271382.1:n.1251+2533_1251+2590dup
XM_005271326.4:c.1207_1239+25dup
XM_005271327.4:c.1024_1056+25dup
NM_001172309.2:c.1249_1281+25dup
NM_144573.4:c.1441_1473+25dup