Canonical Allele Identifier: CA1177631161

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942120_77942126delinsGAGAAGA , CM000663.2:g.77942120_77942126delinsGAGAAGA	GRCh38
NC_000001.10:g.78407805_78407811delinsGAGAAGA , CM000663.1:g.78407805_78407811delinsGAGAAGA	GRCh37
NC_000001.9:g.78180393_78180399delinsGAGAAGA	NCBI36
NG_016625.1:g.58606_58612delinsGAGAAGA , LRG_442:g.58606_58612delinsGAGAAGA
NG_033243.2:g.41968_41974delinsTCTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1571_1577delinsGAGAAGA MANE Select	ENSP00000333938.7:p.Arg524=
ENST00000330010.12:c.1379_1385delinsGAGAAGA	ENSP00000327363.8:p.Arg460=
ENST00000334785.11:c.1571_1577delinsGAGAAGA	ENSP00000333938.7:p.Arg524=
ENST00000342754.5:c.1270_1276delinsGAGAAGA
ENST00000470735.1:n.410_416delinsGAGAAGA
ENST00000480732.2:n.1145_1151delinsGAGAAGA
NM_001172309.1:c.1379_1385delinsGAGAAGA	NP_001165780.1:p.Arg460=
NM_144573.3:c.1571_1577delinsGAGAAGA , LRG_442t1:c.1571_1577delinsGAGAAGA	NP_653174.3:p.Arg524=
XM_005271322.2:c.1571_1577delinsGAGAAGA	XP_005271379.1:p.Arg524=
XM_005271323.2:c.1529_1535delinsGAGAAGA	XP_005271380.1:p.Arg510=
XM_005271324.3:c.1379_1385delinsGAGAAGA	XP_005271381.1:p.Arg460=
XM_005271325.2:c.1349_1355delinsGAGAAGA	XP_005271382.1:p.Arg450=
XM_005271326.2:c.1337_1343delinsGAGAAGA	XP_005271383.1:p.Arg446=
XM_005271327.2:c.1154_1160delinsGAGAAGA	XP_005271384.1:p.Arg385=
XM_005271322.4:c.1571_1577delinsGAGAAGA	XP_005271379.1:p.Arg524=
XM_005271323.4:c.1529_1535delinsGAGAAGA	XP_005271380.1:p.Arg510=
XM_005271324.5:c.1379_1385delinsGAGAAGA	XP_005271381.1:p.Arg460=
XM_005271325.4:c.1349_1355delinsGAGAAGA	XP_005271382.1:p.Arg450=
XM_005271326.4:c.1337_1343delinsGAGAAGA	XP_005271383.1:p.Arg446=
XM_005271327.4:c.1154_1160delinsGAGAAGA	XP_005271384.1:p.Arg385=
NM_001172309.2:c.1379_1385delinsGAGAAGA	NP_001165780.1:p.Arg460=
NM_144573.4:c.1571_1577delinsGAGAAGA MANE Select	NP_653174.3:p.Arg524=