Canonical Allele Identifier: CA2744232126

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935523_77935524insTG , CM000663.2:g.77935523_77935524insTG	GRCh38
NC_000001.10:g.78401208_78401209insTG , CM000663.1:g.78401208_78401209insTG	GRCh37
NC_000001.9:g.78173796_78173797insTG	NCBI36
NG_016625.1:g.52009_52010insTG , LRG_442:g.52009_52010insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-300_1252-299insTG MANE Select	ENSP00000333938.7:n.1252-300_1252-299insTG
ENST00000330010.12:c.1060-300_1060-299insTG	ENSP00000327363.8:n.1060-300_1060-299insTG
ENST00000334785.11:c.1252-300_1252-299insTG	ENSP00000333938.7:n.1252-300_1252-299insTG
ENST00000342754.5:c.951-300_951-299insTG
ENST00000440324.5:c.1210-300_1210-299insTG	ENSP00000411902.1:n.1210-300_1210-299insTG
ENST00000464998.1:n.712-300_712-299insTG
ENST00000480732.2:n.826-300_826-299insTG
NM_001172309.1:c.1060-300_1060-299insTG	NP_001165780.1:n.1060-300_1060-299insTG
NM_144573.3:c.1252-300_1252-299insTG , LRG_442t1:c.1252-300_1252-299insTG	NP_653174.3:n.1252-300_1252-299insTG
XM_005271322.2:c.1252-300_1252-299insTG	XP_005271379.1:n.1252-300_1252-299insTG
XM_005271323.2:c.1210-300_1210-299insTG	XP_005271380.1:n.1210-300_1210-299insTG
XM_005271324.3:c.1060-300_1060-299insTG	XP_005271381.1:n.1060-300_1060-299insTG
XM_005271325.2:c.1251+2044_1251+2045insTG	XP_005271382.1:n.1251+2044_1251+2045insTG
XM_005271326.2:c.1018-300_1018-299insTG	XP_005271383.1:n.1018-300_1018-299insTG
XM_005271327.2:c.835-300_835-299insTG	XP_005271384.1:n.835-300_835-299insTG
XM_005271322.4:c.1252-300_1252-299insTG	XP_005271379.1:n.1252-300_1252-299insTG
XM_005271323.4:c.1210-300_1210-299insTG	XP_005271380.1:n.1210-300_1210-299insTG
XM_005271324.5:c.1060-300_1060-299insTG	XP_005271381.1:n.1060-300_1060-299insTG
XM_005271325.4:c.1251+2044_1251+2045insTG	XP_005271382.1:n.1251+2044_1251+2045insTG
XM_005271326.4:c.1018-300_1018-299insTG	XP_005271383.1:n.1018-300_1018-299insTG
XM_005271327.4:c.835-300_835-299insTG	XP_005271384.1:n.835-300_835-299insTG
NM_001172309.2:c.1060-300_1060-299insTG	NP_001165780.1:n.1060-300_1060-299insTG
NM_144573.4:c.1252-300_1252-299insTG MANE Select	NP_653174.3:n.1252-300_1252-299insTG