Canonical Allele Identifier: CA1177626422

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942938_77942940delinsTTC , CM000663.2:g.77942938_77942940delinsTTC	GRCh38
NC_000001.10:g.78408623_78408625delinsTTC , CM000663.1:g.78408623_78408625delinsTTC	GRCh37
NC_000001.9:g.78181211_78181213delinsTTC	NCBI36
NG_016625.1:g.59424_59426delinsTTC , LRG_442:g.59424_59426delinsTTC
NG_033243.2:g.41154_41156delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*109_*111delinsTTC MANE Select	ENSP00000333938.7:n.*109_*111delinsTTC
ENST00000330010.12:c.*109_*111delinsTTC	ENSP00000327363.8:n.*109_*111delinsTTC
ENST00000334785.11:c.*109_*111delinsTTC	ENSP00000333938.7:n.*109_*111delinsTTC
ENST00000342754.5:c.1755_1757delinsTTC
ENST00000480732.2:n.1711_1713delinsTTC
NM_001172309.1:c.*109_*111delinsTTC	NP_001165780.1:n.*109_*111delinsTTC
NM_144573.3:c.*109_*111delinsTTC , LRG_442t1:c.*109_*111delinsTTC	NP_653174.3:n.*109_*111delinsTTC
XM_005271322.2:c.*25_*27delinsTTC	XP_005271379.1:n.*25_*27delinsTTC
XM_005271323.2:c.*25_*27delinsTTC	XP_005271380.1:n.*25_*27delinsTTC
XM_005271324.3:c.*25_*27delinsTTC	XP_005271381.1:n.*25_*27delinsTTC
XM_005271325.2:c.*25_*27delinsTTC	XP_005271382.1:n.*25_*27delinsTTC
XM_005271326.2:c.*25_*27delinsTTC	XP_005271383.1:n.*25_*27delinsTTC
XM_005271327.2:c.*25_*27delinsTTC	XP_005271384.1:n.*25_*27delinsTTC
XM_005271322.4:c.*25_*27delinsTTC	XP_005271379.1:n.*25_*27delinsTTC
XM_005271323.4:c.*25_*27delinsTTC	XP_005271380.1:n.*25_*27delinsTTC
XM_005271324.5:c.*25_*27delinsTTC	XP_005271381.1:n.*25_*27delinsTTC
XM_005271325.4:c.*25_*27delinsTTC	XP_005271382.1:n.*25_*27delinsTTC
XM_005271326.4:c.*25_*27delinsTTC	XP_005271383.1:n.*25_*27delinsTTC
XM_005271327.4:c.*25_*27delinsTTC	XP_005271384.1:n.*25_*27delinsTTC
NM_001172309.2:c.*109_*111delinsTTC	NP_001165780.1:n.*109_*111delinsTTC
NM_144573.4:c.*109_*111delinsTTC MANE Select	NP_653174.3:n.*109_*111delinsTTC