Canonical Allele Identifier: CA1177626555

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943060_77943061delinsTC , CM000663.2:g.77943060_77943061delinsTC	GRCh38
NC_000001.10:g.78408745_78408746delinsTC , CM000663.1:g.78408745_78408746delinsTC	GRCh37
NC_000001.9:g.78181333_78181334delinsTC	NCBI36
NG_016625.1:g.59546_59547delinsTC , LRG_442:g.59546_59547delinsTC
NG_033243.2:g.41033_41034delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*231_*232delinsTC MANE Select	ENSP00000333938.7:n.*231_*232delinsTC
ENST00000330010.12:c.*231_*232delinsTC	ENSP00000327363.8:n.*231_*232delinsTC
ENST00000334785.11:c.*231_*232delinsTC	ENSP00000333938.7:n.*231_*232delinsTC
ENST00000342754.5:c.1877_1878delinsTC
ENST00000480732.2:n.1833_1834delinsTC
NM_001172309.1:c.*231_*232delinsTC	NP_001165780.1:n.*231_*232delinsTC
NM_144573.3:c.*231_*232delinsTC , LRG_442t1:c.*231_*232delinsTC	NP_653174.3:n.*231_*232delinsTC
XM_005271322.2:c.*147_*148delinsTC	XP_005271379.1:n.*147_*148delinsTC
XM_005271323.2:c.*147_*148delinsTC	XP_005271380.1:n.*147_*148delinsTC
XM_005271324.3:c.*147_*148delinsTC	XP_005271381.1:n.*147_*148delinsTC
XM_005271325.2:c.*147_*148delinsTC	XP_005271382.1:n.*147_*148delinsTC
XM_005271326.2:c.*147_*148delinsTC	XP_005271383.1:n.*147_*148delinsTC
XM_005271327.2:c.*147_*148delinsTC	XP_005271384.1:n.*147_*148delinsTC
XM_005271322.4:c.*147_*148delinsTC	XP_005271379.1:n.*147_*148delinsTC
XM_005271323.4:c.*147_*148delinsTC	XP_005271380.1:n.*147_*148delinsTC
XM_005271324.5:c.*147_*148delinsTC	XP_005271381.1:n.*147_*148delinsTC
XM_005271325.4:c.*147_*148delinsTC	XP_005271382.1:n.*147_*148delinsTC
XM_005271326.4:c.*147_*148delinsTC	XP_005271383.1:n.*147_*148delinsTC
XM_005271327.4:c.*147_*148delinsTC	XP_005271384.1:n.*147_*148delinsTC
NM_001172309.2:c.*231_*232delinsTC	NP_001165780.1:n.*231_*232delinsTC
NM_144573.4:c.*231_*232delinsTC MANE Select	NP_653174.3:n.*231_*232delinsTC