Canonical Allele Identifier: CA2646275776

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942885-TCTTCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942886_77942891del , CM000663.2:g.77942886_77942891del	GRCh38
NC_000001.10:g.78408571_78408576del , CM000663.1:g.78408571_78408576del	GRCh37
NC_000001.9:g.78181159_78181164del	NCBI36
NG_016625.1:g.59372_59377del , LRG_442:g.59372_59377del
NG_033243.2:g.41203_41208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*57_*62del MANE Select	ENSP00000333938.7:n.*57_*62del
ENST00000330010.12:c.*57_*62del	ENSP00000327363.8:n.*57_*62del
ENST00000334785.11:c.*57_*62del	ENSP00000333938.7:n.*57_*62del
ENST00000342754.5:c.1717-14_1717-9del
ENST00000480732.2:n.1659_1664del
NM_001172309.1:c.*57_*62del	NP_001165780.1:n.*57_*62del
NM_144573.3:c.*57_*62del , LRG_442t1:c.*57_*62del	NP_653174.3:n.*57_*62del
XM_005271322.2:c.2018-14_2018-9del	XP_005271379.1:n.2018-14_2018-9del
XM_005271323.2:c.1976-14_1976-9del	XP_005271380.1:n.1976-14_1976-9del
XM_005271324.3:c.1826-14_1826-9del	XP_005271381.1:n.1826-14_1826-9del
XM_005271325.2:c.1796-14_1796-9del	XP_005271382.1:n.1796-14_1796-9del
XM_005271326.2:c.1784-14_1784-9del	XP_005271383.1:n.1784-14_1784-9del
XM_005271327.2:c.1601-14_1601-9del	XP_005271384.1:n.1601-14_1601-9del
XM_005271322.4:c.2018-14_2018-9del	XP_005271379.1:n.2018-14_2018-9del
XM_005271323.4:c.1976-14_1976-9del	XP_005271380.1:n.1976-14_1976-9del
XM_005271324.5:c.1826-14_1826-9del	XP_005271381.1:n.1826-14_1826-9del
XM_005271325.4:c.1796-14_1796-9del	XP_005271382.1:n.1796-14_1796-9del
XM_005271326.4:c.1784-14_1784-9del	XP_005271383.1:n.1784-14_1784-9del
XM_005271327.4:c.1601-14_1601-9del	XP_005271384.1:n.1601-14_1601-9del
NM_001172309.2:c.*57_*62del	NP_001165780.1:n.*57_*62del
NM_144573.4:c.*57_*62del MANE Select	NP_653174.3:n.*57_*62del