Canonical Allele Identifier: CA418572976

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407713T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942028T>C , CM000663.2:g.77942028T>C	GRCh38
NC_000001.10:g.78407713T>C , CM000663.1:g.78407713T>C	GRCh37
NC_000001.9:g.78180301T>C	NCBI36
NG_016625.1:g.58514T>C , LRG_442:g.58514T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1479T>C MANE Select	ENSP00000333938.7:p.Asp493=
ENST00000330010.12:c.1287T>C	ENSP00000327363.8:p.Asp429=
ENST00000334785.11:c.1479T>C	ENSP00000333938.7:p.Asp493=
ENST00000342754.5:c.1178T>C
ENST00000470735.1:n.318T>C
ENST00000480732.2:n.1053T>C
NM_001172309.1:c.1287T>C	NP_001165780.1:p.Asp429=
NM_144573.3:c.1479T>C , LRG_442t1:c.1479T>C	NP_653174.3:p.Asp493=
XM_005271322.2:c.1479T>C	XP_005271379.1:p.Asp493=
XM_005271323.2:c.1437T>C	XP_005271380.1:p.Asp479=
XM_005271324.3:c.1287T>C	XP_005271381.1:p.Asp429=
XM_005271325.2:c.1257T>C	XP_005271382.1:p.Asp419=
XM_005271326.2:c.1245T>C	XP_005271383.1:p.Asp415=
XM_005271327.2:c.1062T>C	XP_005271384.1:p.Asp354=
XM_005271322.4:c.1479T>C	XP_005271379.1:p.Asp493=
XM_005271323.4:c.1437T>C	XP_005271380.1:p.Asp479=
XM_005271324.5:c.1287T>C	XP_005271381.1:p.Asp429=
XM_005271325.4:c.1257T>C	XP_005271382.1:p.Asp419=
XM_005271326.4:c.1245T>C	XP_005271383.1:p.Asp415=
XM_005271327.4:c.1062T>C	XP_005271384.1:p.Asp354=
NM_001172309.2:c.1287T>C	NP_001165780.1:p.Asp429=
NM_144573.4:c.1479T>C MANE Select	NP_653174.3:p.Asp493=