Canonical Allele Identifier: CA1177626259

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942884_77942889delinsTTCTTC , CM000663.2:g.77942884_77942889delinsTTCTTC	GRCh38
NC_000001.10:g.78408569_78408574delinsTTCTTC , CM000663.1:g.78408569_78408574delinsTTCTTC	GRCh37
NC_000001.9:g.78181157_78181162delinsTTCTTC	NCBI36
NG_016625.1:g.59370_59375delinsTTCTTC , LRG_442:g.59370_59375delinsTTCTTC
NG_033243.2:g.41205_41210delinsGAAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*55_*60delinsTTCTTC MANE Select	ENSP00000333938.7:n.*55_*60delinsTTCTTC
ENST00000330010.12:c.*55_*60delinsTTCTTC	ENSP00000327363.8:n.*55_*60delinsTTCTTC
ENST00000334785.11:c.*55_*60delinsTTCTTC	ENSP00000333938.7:n.*55_*60delinsTTCTTC
ENST00000342754.5:c.1717-16_1717-11delinsTTCTTC
ENST00000480732.2:n.1657_1662delinsTTCTTC
NM_001172309.1:c.*55_*60delinsTTCTTC	NP_001165780.1:n.*55_*60delinsTTCTTC
NM_144573.3:c.*55_*60delinsTTCTTC , LRG_442t1:c.*55_*60delinsTTCTTC	NP_653174.3:n.*55_*60delinsTTCTTC
XM_005271322.2:c.2018-16_2018-11delinsTTCTTC	XP_005271379.1:n.2018-16_2018-11delinsTTCTTC
XM_005271323.2:c.1976-16_1976-11delinsTTCTTC	XP_005271380.1:n.1976-16_1976-11delinsTTCTTC
XM_005271324.3:c.1826-16_1826-11delinsTTCTTC	XP_005271381.1:n.1826-16_1826-11delinsTTCTTC
XM_005271325.2:c.1796-16_1796-11delinsTTCTTC	XP_005271382.1:n.1796-16_1796-11delinsTTCTTC
XM_005271326.2:c.1784-16_1784-11delinsTTCTTC	XP_005271383.1:n.1784-16_1784-11delinsTTCTTC
XM_005271327.2:c.1601-16_1601-11delinsTTCTTC	XP_005271384.1:n.1601-16_1601-11delinsTTCTTC
XM_005271322.4:c.2018-16_2018-11delinsTTCTTC	XP_005271379.1:n.2018-16_2018-11delinsTTCTTC
XM_005271323.4:c.1976-16_1976-11delinsTTCTTC	XP_005271380.1:n.1976-16_1976-11delinsTTCTTC
XM_005271324.5:c.1826-16_1826-11delinsTTCTTC	XP_005271381.1:n.1826-16_1826-11delinsTTCTTC
XM_005271325.4:c.1796-16_1796-11delinsTTCTTC	XP_005271382.1:n.1796-16_1796-11delinsTTCTTC
XM_005271326.4:c.1784-16_1784-11delinsTTCTTC	XP_005271383.1:n.1784-16_1784-11delinsTTCTTC
XM_005271327.4:c.1601-16_1601-11delinsTTCTTC	XP_005271384.1:n.1601-16_1601-11delinsTTCTTC
NM_001172309.2:c.*55_*60delinsTTCTTC	NP_001165780.1:n.*55_*60delinsTTCTTC
NM_144573.4:c.*55_*60delinsTTCTTC MANE Select	NP_653174.3:n.*55_*60delinsTTCTTC