Canonical Allele Identifier: CA1177631469

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942766A= , CM000663.2:g.77942766A=	GRCh38
NC_000001.10:g.78408451A= , CM000663.1:g.78408451A=	GRCh37
NC_000001.9:g.78181039A=	NCBI36
NG_016625.1:g.59252A= , LRG_442:g.59252A=
NG_033243.2:g.41328T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1965A= MANE Select	ENSP00000333938.7:p.Lys655=
ENST00000330010.12:c.1773A=	ENSP00000327363.8:p.Lys591=
ENST00000334785.11:c.1965A=	ENSP00000333938.7:p.Lys655=
ENST00000342754.5:c.1664A=
ENST00000480732.2:n.1539A=
NM_001172309.1:c.1773A=	NP_001165780.1:p.Lys591=
NM_144573.3:c.1965A= , LRG_442t1:c.1965A=	NP_653174.3:p.Lys655=
XM_005271322.2:c.1965A=	XP_005271379.1:p.Lys655=
XM_005271323.2:c.1923A=	XP_005271380.1:p.Lys641=
XM_005271324.3:c.1773A=	XP_005271381.1:p.Lys591=
XM_005271325.2:c.1743A=	XP_005271382.1:p.Lys581=
XM_005271326.2:c.1731A=	XP_005271383.1:p.Lys577=
XM_005271327.2:c.1548A=	XP_005271384.1:p.Lys516=
XM_005271322.4:c.1965A=	XP_005271379.1:p.Lys655=
XM_005271323.4:c.1923A=	XP_005271380.1:p.Lys641=
XM_005271324.5:c.1773A=	XP_005271381.1:p.Lys591=
XM_005271325.4:c.1743A=	XP_005271382.1:p.Lys581=
XM_005271326.4:c.1731A=	XP_005271383.1:p.Lys577=
XM_005271327.4:c.1548A=	XP_005271384.1:p.Lys516=
NM_001172309.2:c.1773A=	NP_001165780.1:p.Lys591=
NM_144573.4:c.1965A= MANE Select	NP_653174.3:p.Lys655=