Canonical Allele Identifier: CA340875970

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77929500A>G , CM000663.2:g.77929500A>G	GRCh38
NC_000001.10:g.78395185A>G , CM000663.1:g.78395185A>G	GRCh37
NC_000001.9:g.78167773A>G	NCBI36
NG_016625.1:g.45986A>G , LRG_442:g.45986A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_144573.4:c.1049A>G MANE Select	NP_653174.3:p.Asn350Ser
ENST00000334785.12:c.1049A>G MANE Select	ENSP00000333938.7:p.Asn350Ser
NM_001172309.1:c.857A>G	NP_001165780.1:p.Asn286Ser
NM_001172309.2:c.857A>G	NP_001165780.1:p.Asn286Ser
NM_144573.3:c.1049A>G , LRG_442t1:c.1049A>G	NP_653174.3:p.Asn350Ser
ENST00000330010.12:c.857A>G	ENSP00000327363.8:p.Asn286Ser
ENST00000334785.11:c.1049A>G	ENSP00000333938.7:p.Asn350Ser
ENST00000342754.5:c.748A>G
ENST00000401035.7:c.857A>G	ENSP00000383814.3:p.Asn286Ser
ENST00000440324.5:c.1007A>G	ENSP00000411902.1:p.Asn336Ser
ENST00000464998.1:n.509A>G
XM_005271322.2:c.1049A>G	XP_005271379.1:p.Asn350Ser
XM_005271322.4:c.1049A>G	XP_005271379.1:p.Asn350Ser
XM_005271323.2:c.1007A>G	XP_005271380.1:p.Asn336Ser
XM_005271323.4:c.1007A>G	XP_005271380.1:p.Asn336Ser
XM_005271324.3:c.857A>G	XP_005271381.1:p.Asn286Ser
XM_005271324.5:c.857A>G	XP_005271381.1:p.Asn286Ser
XM_005271325.2:c.1049A>G	XP_005271382.1:p.Asn350Ser
XM_005271325.4:c.1049A>G	XP_005271382.1:p.Asn350Ser
XM_005271326.2:c.815A>G	XP_005271383.1:p.Asn272Ser
XM_005271326.4:c.815A>G	XP_005271383.1:p.Asn272Ser
XM_005271327.2:c.632A>G	XP_005271384.1:p.Asn211Ser
XM_005271327.4:c.632A>G	XP_005271384.1:p.Asn211Ser