Canonical Allele Identifier: CA1177631210

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942203_77942204delinsCA , CM000663.2:g.77942203_77942204delinsCA	GRCh38
NC_000001.10:g.78407888_78407889delinsCA , CM000663.1:g.78407888_78407889delinsCA	GRCh37
NC_000001.9:g.78180476_78180477delinsCA	NCBI36
NG_016625.1:g.58689_58690delinsCA , LRG_442:g.58689_58690delinsCA
NG_033243.2:g.41890_41891delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1654_1655delinsCA MANE Select	ENSP00000333938.7:p.Gln552=
ENST00000330010.12:c.1462_1463delinsCA	ENSP00000327363.8:p.Gln488=
ENST00000334785.11:c.1654_1655delinsCA	ENSP00000333938.7:p.Gln552=
ENST00000342754.5:c.1353_1354delinsCA
ENST00000470735.1:n.493_494delinsCA
ENST00000480732.2:n.1228_1229delinsCA
NM_001172309.1:c.1462_1463delinsCA	NP_001165780.1:p.Gln488=
NM_144573.3:c.1654_1655delinsCA , LRG_442t1:c.1654_1655delinsCA	NP_653174.3:p.Gln552=
XM_005271322.2:c.1654_1655delinsCA	XP_005271379.1:p.Gln552=
XM_005271323.2:c.1612_1613delinsCA	XP_005271380.1:p.Gln538=
XM_005271324.3:c.1462_1463delinsCA	XP_005271381.1:p.Gln488=
XM_005271325.2:c.1432_1433delinsCA	XP_005271382.1:p.Gln478=
XM_005271326.2:c.1420_1421delinsCA	XP_005271383.1:p.Gln474=
XM_005271327.2:c.1237_1238delinsCA	XP_005271384.1:p.Gln413=
XM_005271322.4:c.1654_1655delinsCA	XP_005271379.1:p.Gln552=
XM_005271323.4:c.1612_1613delinsCA	XP_005271380.1:p.Gln538=
XM_005271324.5:c.1462_1463delinsCA	XP_005271381.1:p.Gln488=
XM_005271325.4:c.1432_1433delinsCA	XP_005271382.1:p.Gln478=
XM_005271326.4:c.1420_1421delinsCA	XP_005271383.1:p.Gln474=
XM_005271327.4:c.1237_1238delinsCA	XP_005271384.1:p.Gln413=
NM_001172309.2:c.1462_1463delinsCA	NP_001165780.1:p.Gln488=
NM_144573.4:c.1654_1655delinsCA MANE Select	NP_653174.3:p.Gln552=