Canonical Allele Identifier: CA1148261227

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942890_77942894delinsTCTTT , CM000663.2:g.77942890_77942894delinsTCTTT	GRCh38
NC_000001.10:g.78408575_78408579delinsTCTTT , CM000663.1:g.78408575_78408579delinsTCTTT	GRCh37
NC_000001.9:g.78181163_78181167delinsTCTTT	NCBI36
NG_016625.1:g.59376_59380delinsTCTTT , LRG_442:g.59376_59380delinsTCTTT
NG_033243.2:g.41200_41204delinsAAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*61_*65delinsTCTTT MANE Select	ENSP00000333938.7:n.*61_*65delinsTCTTT
ENST00000330010.12:c.*61_*65delinsTCTTT	ENSP00000327363.8:n.*61_*65delinsTCTTT
ENST00000334785.11:c.*61_*65delinsTCTTT	ENSP00000333938.7:n.*61_*65delinsTCTTT
ENST00000342754.5:c.1717-10_1717-6delinsTCTTT
ENST00000480732.2:n.1663_1667delinsTCTTT
NM_001172309.1:c.*61_*65delinsTCTTT	NP_001165780.1:n.*61_*65delinsTCTTT
NM_144573.3:c.*61_*65delinsTCTTT , LRG_442t1:c.*61_*65delinsTCTTT	NP_653174.3:n.*61_*65delinsTCTTT
XM_005271322.2:c.2018-10_2018-6delinsTCTTT	XP_005271379.1:n.2018-10_2018-6delinsTCTTT
XM_005271323.2:c.1976-10_1976-6delinsTCTTT	XP_005271380.1:n.1976-10_1976-6delinsTCTTT
XM_005271324.3:c.1826-10_1826-6delinsTCTTT	XP_005271381.1:n.1826-10_1826-6delinsTCTTT
XM_005271325.2:c.1796-10_1796-6delinsTCTTT	XP_005271382.1:n.1796-10_1796-6delinsTCTTT
XM_005271326.2:c.1784-10_1784-6delinsTCTTT	XP_005271383.1:n.1784-10_1784-6delinsTCTTT
XM_005271327.2:c.1601-10_1601-6delinsTCTTT	XP_005271384.1:n.1601-10_1601-6delinsTCTTT
XM_005271322.4:c.2018-10_2018-6delinsTCTTT	XP_005271379.1:n.2018-10_2018-6delinsTCTTT
XM_005271323.4:c.1976-10_1976-6delinsTCTTT	XP_005271380.1:n.1976-10_1976-6delinsTCTTT
XM_005271324.5:c.1826-10_1826-6delinsTCTTT	XP_005271381.1:n.1826-10_1826-6delinsTCTTT
XM_005271325.4:c.1796-10_1796-6delinsTCTTT	XP_005271382.1:n.1796-10_1796-6delinsTCTTT
XM_005271326.4:c.1784-10_1784-6delinsTCTTT	XP_005271383.1:n.1784-10_1784-6delinsTCTTT
XM_005271327.4:c.1601-10_1601-6delinsTCTTT	XP_005271384.1:n.1601-10_1601-6delinsTCTTT
NM_001172309.2:c.*61_*65delinsTCTTT	NP_001165780.1:n.*61_*65delinsTCTTT
NM_144573.4:c.*61_*65delinsTCTTT MANE Select	NP_653174.3:n.*61_*65delinsTCTTT