Canonical Allele Identifier: CA1146358702
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77943041_77943043delinsACA , CM000663.2:g.77943041_77943043delinsACA GRCh38
NC_000001.10:g.78408726_78408728delinsACA , CM000663.1:g.78408726_78408728delinsACA GRCh37
NC_000001.9:g.78181314_78181316delinsACA NCBI36
NG_016625.1:g.59527_59529delinsACA , LRG_442:g.59527_59529delinsACA
NG_033243.2:g.41051_41053delinsTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.*212_*214delinsACA MANE Select ENSP00000333938.7:n.*212_*214delinsACA
ENST00000330010.12:c.*212_*214delinsACA ENSP00000327363.8:n.*212_*214delinsACA
ENST00000334785.11:c.*212_*214delinsACA ENSP00000333938.7:n.*212_*214delinsACA
ENST00000342754.5:c.1858_1860delinsACA
ENST00000480732.2:n.1814_1816delinsACA
NM_001172309.1:c.*212_*214delinsACA NP_001165780.1:n.*212_*214delinsACA
NM_144573.3:c.*212_*214delinsACA , LRG_442t1:c.*212_*214delinsACA NP_653174.3:n.*212_*214delinsACA
XM_005271322.2:c.*128_*130delinsACA XP_005271379.1:n.*128_*130delinsACA
XM_005271323.2:c.*128_*130delinsACA XP_005271380.1:n.*128_*130delinsACA
XM_005271324.3:c.*128_*130delinsACA XP_005271381.1:n.*128_*130delinsACA
XM_005271325.2:c.*128_*130delinsACA XP_005271382.1:n.*128_*130delinsACA
XM_005271326.2:c.*128_*130delinsACA XP_005271383.1:n.*128_*130delinsACA
XM_005271327.2:c.*128_*130delinsACA XP_005271384.1:n.*128_*130delinsACA
XM_005271322.4:c.*128_*130delinsACA XP_005271379.1:n.*128_*130delinsACA
XM_005271323.4:c.*128_*130delinsACA XP_005271380.1:n.*128_*130delinsACA
XM_005271324.5:c.*128_*130delinsACA XP_005271381.1:n.*128_*130delinsACA
XM_005271325.4:c.*128_*130delinsACA XP_005271382.1:n.*128_*130delinsACA
XM_005271326.4:c.*128_*130delinsACA XP_005271383.1:n.*128_*130delinsACA
XM_005271327.4:c.*128_*130delinsACA XP_005271384.1:n.*128_*130delinsACA
NM_001172309.2:c.*212_*214delinsACA NP_001165780.1:n.*212_*214delinsACA
NM_144573.4:c.*212_*214delinsACA MANE Select NP_653174.3:n.*212_*214delinsACA