Canonical Allele Identifier: CA2739708122

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942905G>C , CM000663.2:g.77942905G>C	GRCh38
NC_000001.10:g.78408590G>C , CM000663.1:g.78408590G>C	GRCh37
NC_000001.9:g.78181178G>C	NCBI36
NG_016625.1:g.59391G>C , LRG_442:g.59391G>C
NG_033243.2:g.41189C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*76G>C MANE Select	ENSP00000333938.7:n.*76G>C
ENST00000330010.12:c.*76G>C	ENSP00000327363.8:n.*76G>C
ENST00000334785.11:c.*76G>C	ENSP00000333938.7:n.*76G>C
ENST00000342754.5:c.1722G>C
ENST00000480732.2:n.1678G>C
NM_001172309.1:c.*76G>C	NP_001165780.1:n.*76G>C
NM_144573.3:c.*76G>C , LRG_442t1:c.*76G>C	NP_653174.3:n.*76G>C
XM_005271322.2:c.2023G>C	XP_005271379.1:p.Asp675His
XM_005271323.2:c.1981G>C	XP_005271380.1:p.Asp661His
XM_005271324.3:c.1831G>C	XP_005271381.1:p.Asp611His
XM_005271325.2:c.1801G>C	XP_005271382.1:p.Asp601His
XM_005271326.2:c.1789G>C	XP_005271383.1:p.Asp597His
XM_005271327.2:c.1606G>C	XP_005271384.1:p.Asp536His
XM_005271322.4:c.2023G>C	XP_005271379.1:p.Asp675His
XM_005271323.4:c.1981G>C	XP_005271380.1:p.Asp661His
XM_005271324.5:c.1831G>C	XP_005271381.1:p.Asp611His
XM_005271325.4:c.1801G>C	XP_005271382.1:p.Asp601His
XM_005271326.4:c.1789G>C	XP_005271383.1:p.Asp597His
XM_005271327.4:c.1606G>C	XP_005271384.1:p.Asp536His
NM_001172309.2:c.*76G>C	NP_001165780.1:n.*76G>C
NM_144573.4:c.*76G>C MANE Select	NP_653174.3:n.*76G>C