Canonical Allele Identifier: CA1177631223

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942246C= , CM000663.2:g.77942246C=	GRCh38
NC_000001.10:g.78407931C= , CM000663.1:g.78407931C=	GRCh37
NC_000001.9:g.78180519C=	NCBI36
NG_016625.1:g.58732C= , LRG_442:g.58732C=
NG_033243.2:g.41848G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1659+38C= MANE Select	ENSP00000333938.7:n.1659+38C=
ENST00000330010.12:c.1467+38C=	ENSP00000327363.8:n.1467+38C=
ENST00000334785.11:c.1659+38C=	ENSP00000333938.7:n.1659+38C=
ENST00000342754.5:c.1358+38C=
ENST00000470735.1:n.498+38C=
ENST00000480732.2:n.1233+38C=
NM_001172309.1:c.1467+38C=	NP_001165780.1:n.1467+38C=
NM_144573.3:c.1659+38C= , LRG_442t1:c.1659+38C=	NP_653174.3:n.1659+38C=
XM_005271322.2:c.1659+38C=	XP_005271379.1:n.1659+38C=
XM_005271323.2:c.1617+38C=	XP_005271380.1:n.1617+38C=
XM_005271324.3:c.1467+38C=	XP_005271381.1:n.1467+38C=
XM_005271325.2:c.1437+38C=	XP_005271382.1:n.1437+38C=
XM_005271326.2:c.1425+38C=	XP_005271383.1:n.1425+38C=
XM_005271327.2:c.1242+38C=	XP_005271384.1:n.1242+38C=
XM_005271322.4:c.1659+38C=	XP_005271379.1:n.1659+38C=
XM_005271323.4:c.1617+38C=	XP_005271380.1:n.1617+38C=
XM_005271324.5:c.1467+38C=	XP_005271381.1:n.1467+38C=
XM_005271325.4:c.1437+38C=	XP_005271382.1:n.1437+38C=
XM_005271326.4:c.1425+38C=	XP_005271383.1:n.1425+38C=
XM_005271327.4:c.1242+38C=	XP_005271384.1:n.1242+38C=
NM_001172309.2:c.1467+38C=	NP_001165780.1:n.1467+38C=
NM_144573.4:c.1659+38C= MANE Select	NP_653174.3:n.1659+38C=