Canonical Allele Identifier: CA2525338688

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933499_77933500insCAG , CM000663.2:g.77933499_77933500insCAG	GRCh38
NC_000001.10:g.78399184_78399185insCAG , CM000663.1:g.78399184_78399185insCAG	GRCh37
NC_000001.9:g.78171772_78171773insCAG	NCBI36
NG_016625.1:g.49985_49986insCAG , LRG_442:g.49985_49986insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+20_1251+21insCAG MANE Select	ENSP00000333938.7:n.1251+20_1251+21insCAG
ENST00000330010.12:c.1059+20_1059+21insCAG	ENSP00000327363.8:n.1059+20_1059+21insCAG
ENST00000334785.11:c.1251+20_1251+21insCAG	ENSP00000333938.7:n.1251+20_1251+21insCAG
ENST00000342754.5:c.950+20_950+21insCAG
ENST00000440324.5:c.1209+20_1209+21insCAG	ENSP00000411902.1:n.1209+20_1209+21insCAG
ENST00000464998.1:n.711+20_711+21insCAG
ENST00000480732.2:n.825+20_825+21insCAG
NM_001172309.1:c.1059+20_1059+21insCAG	NP_001165780.1:n.1059+20_1059+21insCAG
NM_144573.3:c.1251+20_1251+21insCAG , LRG_442t1:c.1251+20_1251+21insCAG	NP_653174.3:n.1251+20_1251+21insCAG
XM_005271322.2:c.1251+20_1251+21insCAG	XP_005271379.1:n.1251+20_1251+21insCAG
XM_005271323.2:c.1209+20_1209+21insCAG	XP_005271380.1:n.1209+20_1209+21insCAG
XM_005271324.3:c.1059+20_1059+21insCAG	XP_005271381.1:n.1059+20_1059+21insCAG
XM_005271325.2:c.1251+20_1251+21insCAG	XP_005271382.1:n.1251+20_1251+21insCAG
XM_005271326.2:c.1017+20_1017+21insCAG	XP_005271383.1:n.1017+20_1017+21insCAG
XM_005271327.2:c.834+20_834+21insCAG	XP_005271384.1:n.834+20_834+21insCAG
XM_005271322.4:c.1251+20_1251+21insCAG	XP_005271379.1:n.1251+20_1251+21insCAG
XM_005271323.4:c.1209+20_1209+21insCAG	XP_005271380.1:n.1209+20_1209+21insCAG
XM_005271324.5:c.1059+20_1059+21insCAG	XP_005271381.1:n.1059+20_1059+21insCAG
XM_005271325.4:c.1251+20_1251+21insCAG	XP_005271382.1:n.1251+20_1251+21insCAG
XM_005271326.4:c.1017+20_1017+21insCAG	XP_005271383.1:n.1017+20_1017+21insCAG
XM_005271327.4:c.834+20_834+21insCAG	XP_005271384.1:n.834+20_834+21insCAG
NM_001172309.2:c.1059+20_1059+21insCAG	NP_001165780.1:n.1059+20_1059+21insCAG
NM_144573.4:c.1251+20_1251+21insCAG MANE Select	NP_653174.3:n.1251+20_1251+21insCAG