Canonical Allele Identifier: CA1177626545

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943048_77943059delinsTCAAAGCACAGC , CM000663.2:g.77943048_77943059delinsTCAAAGCACAGC	GRCh38
NC_000001.10:g.78408733_78408744delinsTCAAAGCACAGC , CM000663.1:g.78408733_78408744delinsTCAAAGCACAGC	GRCh37
NC_000001.9:g.78181321_78181332delinsTCAAAGCACAGC	NCBI36
NG_016625.1:g.59534_59545delinsTCAAAGCACAGC , LRG_442:g.59534_59545delinsTCAAAGCACAGC
NG_033243.2:g.41035_41046delinsGCTGTGCTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*219_*230delinsTCAAAGCACAGC MANE Select	ENSP00000333938.7:n.*219_*230delinsTCAAAGCACAGC
ENST00000330010.12:c.*219_*230delinsTCAAAGCACAGC	ENSP00000327363.8:n.*219_*230delinsTCAAAGCACAGC
ENST00000334785.11:c.*219_*230delinsTCAAAGCACAGC	ENSP00000333938.7:n.*219_*230delinsTCAAAGCACAGC
ENST00000342754.5:c.1865_1876delinsTCAAAGCACAGC
ENST00000480732.2:n.1821_1832delinsTCAAAGCACAGC
NM_001172309.1:c.*219_*230delinsTCAAAGCACAGC	NP_001165780.1:n.*219_*230delinsTCAAAGCACAGC
NM_144573.3:c.*219_*230delinsTCAAAGCACAGC , LRG_442t1:c.*219_*230delinsTCAAAGCACAGC	NP_653174.3:n.*219_*230delinsTCAAAGCACAGC
XM_005271322.2:c.*135_*146delinsTCAAAGCACAGC	XP_005271379.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271323.2:c.*135_*146delinsTCAAAGCACAGC	XP_005271380.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271324.3:c.*135_*146delinsTCAAAGCACAGC	XP_005271381.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271325.2:c.*135_*146delinsTCAAAGCACAGC	XP_005271382.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271326.2:c.*135_*146delinsTCAAAGCACAGC	XP_005271383.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271327.2:c.*135_*146delinsTCAAAGCACAGC	XP_005271384.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271322.4:c.*135_*146delinsTCAAAGCACAGC	XP_005271379.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271323.4:c.*135_*146delinsTCAAAGCACAGC	XP_005271380.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271324.5:c.*135_*146delinsTCAAAGCACAGC	XP_005271381.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271325.4:c.*135_*146delinsTCAAAGCACAGC	XP_005271382.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271326.4:c.*135_*146delinsTCAAAGCACAGC	XP_005271383.1:n.*135_*146delinsTCAAAGCACAGC
XM_005271327.4:c.*135_*146delinsTCAAAGCACAGC	XP_005271384.1:n.*135_*146delinsTCAAAGCACAGC
NM_001172309.2:c.*219_*230delinsTCAAAGCACAGC	NP_001165780.1:n.*219_*230delinsTCAAAGCACAGC
NM_144573.4:c.*219_*230delinsTCAAAGCACAGC MANE Select	NP_653174.3:n.*219_*230delinsTCAAAGCACAGC