Canonical Allele Identifier: CA2744247084

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942867_77942868insTT , CM000663.2:g.77942867_77942868insTT	GRCh38
NC_000001.10:g.78408552_78408553insTT , CM000663.1:g.78408552_78408553insTT	GRCh37
NC_000001.9:g.78181140_78181141insTT	NCBI36
NG_016625.1:g.59353_59354insTT , LRG_442:g.59353_59354insTT
NG_033243.2:g.41226_41227insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*38_*39insTT MANE Select	ENSP00000333938.7:n.*38_*39insTT
ENST00000330010.12:c.*38_*39insTT	ENSP00000327363.8:n.*38_*39insTT
ENST00000334785.11:c.*38_*39insTT	ENSP00000333938.7:n.*38_*39insTT
ENST00000342754.5:c.1717-33_1717-32insTT
ENST00000480732.2:n.1640_1641insTT
NM_001172309.1:c.*38_*39insTT	NP_001165780.1:n.*38_*39insTT
NM_144573.3:c.*38_*39insTT , LRG_442t1:c.*38_*39insTT	NP_653174.3:n.*38_*39insTT
XM_005271322.2:c.2018-33_2018-32insTT	XP_005271379.1:n.2018-33_2018-32insTT
XM_005271323.2:c.1976-33_1976-32insTT	XP_005271380.1:n.1976-33_1976-32insTT
XM_005271324.3:c.1826-33_1826-32insTT	XP_005271381.1:n.1826-33_1826-32insTT
XM_005271325.2:c.1796-33_1796-32insTT	XP_005271382.1:n.1796-33_1796-32insTT
XM_005271326.2:c.1784-33_1784-32insTT	XP_005271383.1:n.1784-33_1784-32insTT
XM_005271327.2:c.1601-33_1601-32insTT	XP_005271384.1:n.1601-33_1601-32insTT
XM_005271322.4:c.2018-33_2018-32insTT	XP_005271379.1:n.2018-33_2018-32insTT
XM_005271323.4:c.1976-33_1976-32insTT	XP_005271380.1:n.1976-33_1976-32insTT
XM_005271324.5:c.1826-33_1826-32insTT	XP_005271381.1:n.1826-33_1826-32insTT
XM_005271325.4:c.1796-33_1796-32insTT	XP_005271382.1:n.1796-33_1796-32insTT
XM_005271326.4:c.1784-33_1784-32insTT	XP_005271383.1:n.1784-33_1784-32insTT
XM_005271327.4:c.1601-33_1601-32insTT	XP_005271384.1:n.1601-33_1601-32insTT
NM_001172309.2:c.*38_*39insTT	NP_001165780.1:n.*38_*39insTT
NM_144573.4:c.*38_*39insTT MANE Select	NP_653174.3:n.*38_*39insTT