Canonical Allele Identifier: CA1177626326

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942906_77942907delinsAC , CM000663.2:g.77942906_77942907delinsAC	GRCh38
NC_000001.10:g.78408591_78408592delinsAC , CM000663.1:g.78408591_78408592delinsAC	GRCh37
NC_000001.9:g.78181179_78181180delinsAC	NCBI36
NG_016625.1:g.59392_59393delinsAC , LRG_442:g.59392_59393delinsAC
NG_033243.2:g.41187_41188delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*77_*78delinsAC MANE Select	ENSP00000333938.7:n.*77_*78delinsAC
ENST00000330010.12:c.*77_*78delinsAC	ENSP00000327363.8:n.*77_*78delinsAC
ENST00000334785.11:c.*77_*78delinsAC	ENSP00000333938.7:n.*77_*78delinsAC
ENST00000342754.5:c.1723_1724delinsAC
ENST00000480732.2:n.1679_1680delinsAC
NM_001172309.1:c.*77_*78delinsAC	NP_001165780.1:n.*77_*78delinsAC
NM_144573.3:c.*77_*78delinsAC , LRG_442t1:c.*77_*78delinsAC	NP_653174.3:n.*77_*78delinsAC
XM_005271322.2:c.2024_2025delinsAC	XP_005271379.1:p.Asp675=
XM_005271323.2:c.1982_1983delinsAC	XP_005271380.1:p.Asp661=
XM_005271324.3:c.1832_1833delinsAC	XP_005271381.1:p.Asp611=
XM_005271325.2:c.1802_1803delinsAC	XP_005271382.1:p.Asp601=
XM_005271326.2:c.1790_1791delinsAC	XP_005271383.1:p.Asp597=
XM_005271327.2:c.1607_1608delinsAC	XP_005271384.1:p.Asp536=
XM_005271322.4:c.2024_2025delinsAC	XP_005271379.1:p.Asp675=
XM_005271323.4:c.1982_1983delinsAC	XP_005271380.1:p.Asp661=
XM_005271324.5:c.1832_1833delinsAC	XP_005271381.1:p.Asp611=
XM_005271325.4:c.1802_1803delinsAC	XP_005271382.1:p.Asp601=
XM_005271326.4:c.1790_1791delinsAC	XP_005271383.1:p.Asp597=
XM_005271327.4:c.1607_1608delinsAC	XP_005271384.1:p.Asp536=
NM_001172309.2:c.*77_*78delinsAC	NP_001165780.1:n.*77_*78delinsAC
NM_144573.4:c.*77_*78delinsAC MANE Select	NP_653174.3:n.*77_*78delinsAC