Canonical Allele Identifier: CA1177626532

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943036_77943037delinsTC , CM000663.2:g.77943036_77943037delinsTC	GRCh38
NC_000001.10:g.78408721_78408722delinsTC , CM000663.1:g.78408721_78408722delinsTC	GRCh37
NC_000001.9:g.78181309_78181310delinsTC	NCBI36
NG_016625.1:g.59522_59523delinsTC , LRG_442:g.59522_59523delinsTC
NG_033243.2:g.41057_41058delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*207_*208delinsTC MANE Select	ENSP00000333938.7:n.*207_*208delinsTC
ENST00000330010.12:c.*207_*208delinsTC	ENSP00000327363.8:n.*207_*208delinsTC
ENST00000334785.11:c.*207_*208delinsTC	ENSP00000333938.7:n.*207_*208delinsTC
ENST00000342754.5:c.1853_1854delinsTC
ENST00000480732.2:n.1809_1810delinsTC
NM_001172309.1:c.*207_*208delinsTC	NP_001165780.1:n.*207_*208delinsTC
NM_144573.3:c.*207_*208delinsTC , LRG_442t1:c.*207_*208delinsTC	NP_653174.3:n.*207_*208delinsTC
XM_005271322.2:c.*123_*124delinsTC	XP_005271379.1:n.*123_*124delinsTC
XM_005271323.2:c.*123_*124delinsTC	XP_005271380.1:n.*123_*124delinsTC
XM_005271324.3:c.*123_*124delinsTC	XP_005271381.1:n.*123_*124delinsTC
XM_005271325.2:c.*123_*124delinsTC	XP_005271382.1:n.*123_*124delinsTC
XM_005271326.2:c.*123_*124delinsTC	XP_005271383.1:n.*123_*124delinsTC
XM_005271327.2:c.*123_*124delinsTC	XP_005271384.1:n.*123_*124delinsTC
XM_005271322.4:c.*123_*124delinsTC	XP_005271379.1:n.*123_*124delinsTC
XM_005271323.4:c.*123_*124delinsTC	XP_005271380.1:n.*123_*124delinsTC
XM_005271324.5:c.*123_*124delinsTC	XP_005271381.1:n.*123_*124delinsTC
XM_005271325.4:c.*123_*124delinsTC	XP_005271382.1:n.*123_*124delinsTC
XM_005271326.4:c.*123_*124delinsTC	XP_005271383.1:n.*123_*124delinsTC
XM_005271327.4:c.*123_*124delinsTC	XP_005271384.1:n.*123_*124delinsTC
NM_001172309.2:c.*207_*208delinsTC	NP_001165780.1:n.*207_*208delinsTC
NM_144573.4:c.*207_*208delinsTC MANE Select	NP_653174.3:n.*207_*208delinsTC