Canonical Allele Identifier: CA1177626386

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942935_77942941delinsACTTTCT , CM000663.2:g.77942935_77942941delinsACTTTCT	GRCh38
NC_000001.10:g.78408620_78408626delinsACTTTCT , CM000663.1:g.78408620_78408626delinsACTTTCT	GRCh37
NC_000001.9:g.78181208_78181214delinsACTTTCT	NCBI36
NG_016625.1:g.59421_59427delinsACTTTCT , LRG_442:g.59421_59427delinsACTTTCT
NG_033243.2:g.41153_41159delinsAGAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*106_*112delinsACTTTCT MANE Select	ENSP00000333938.7:n.*106_*112delinsACTTTCT
ENST00000330010.12:c.*106_*112delinsACTTTCT	ENSP00000327363.8:n.*106_*112delinsACTTTCT
ENST00000334785.11:c.*106_*112delinsACTTTCT	ENSP00000333938.7:n.*106_*112delinsACTTTCT
ENST00000342754.5:c.1752_1758delinsACTTTCT
ENST00000480732.2:n.1708_1714delinsACTTTCT
NM_001172309.1:c.*106_*112delinsACTTTCT	NP_001165780.1:n.*106_*112delinsACTTTCT
NM_144573.3:c.*106_*112delinsACTTTCT , LRG_442t1:c.*106_*112delinsACTTTCT	NP_653174.3:n.*106_*112delinsACTTTCT
XM_005271322.2:c.*22_*28delinsACTTTCT	XP_005271379.1:n.*22_*28delinsACTTTCT
XM_005271323.2:c.*22_*28delinsACTTTCT	XP_005271380.1:n.*22_*28delinsACTTTCT
XM_005271324.3:c.*22_*28delinsACTTTCT	XP_005271381.1:n.*22_*28delinsACTTTCT
XM_005271325.2:c.*22_*28delinsACTTTCT	XP_005271382.1:n.*22_*28delinsACTTTCT
XM_005271326.2:c.*22_*28delinsACTTTCT	XP_005271383.1:n.*22_*28delinsACTTTCT
XM_005271327.2:c.*22_*28delinsACTTTCT	XP_005271384.1:n.*22_*28delinsACTTTCT
XM_005271322.4:c.*22_*28delinsACTTTCT	XP_005271379.1:n.*22_*28delinsACTTTCT
XM_005271323.4:c.*22_*28delinsACTTTCT	XP_005271380.1:n.*22_*28delinsACTTTCT
XM_005271324.5:c.*22_*28delinsACTTTCT	XP_005271381.1:n.*22_*28delinsACTTTCT
XM_005271325.4:c.*22_*28delinsACTTTCT	XP_005271382.1:n.*22_*28delinsACTTTCT
XM_005271326.4:c.*22_*28delinsACTTTCT	XP_005271383.1:n.*22_*28delinsACTTTCT
XM_005271327.4:c.*22_*28delinsACTTTCT	XP_005271384.1:n.*22_*28delinsACTTTCT
NM_001172309.2:c.*106_*112delinsACTTTCT	NP_001165780.1:n.*106_*112delinsACTTTCT
NM_144573.4:c.*106_*112delinsACTTTCT MANE Select	NP_653174.3:n.*106_*112delinsACTTTCT