Canonical Allele Identifier: CA340879056

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401626A>T (hg19) ; chr1:g.77935941A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935941A>T , CM000663.2:g.77935941A>T	GRCh38
NC_000001.10:g.78401626A>T , CM000663.1:g.78401626A>T	GRCh37
NC_000001.9:g.78174214A>T	NCBI36
NG_016625.1:g.52427A>T , LRG_442:g.52427A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1370A>T MANE Select	ENSP00000333938.7:p.Gln457Leu
ENST00000330010.12:c.1178A>T	ENSP00000327363.8:p.Gln393Leu
ENST00000334785.11:c.1370A>T	ENSP00000333938.7:p.Gln457Leu
ENST00000342754.5:c.1069A>T
ENST00000464998.1:n.830A>T
ENST00000480732.2:n.944A>T
NM_001172309.1:c.1178A>T	NP_001165780.1:p.Gln393Leu
NM_144573.3:c.1370A>T , LRG_442t1:c.1370A>T	NP_653174.3:p.Gln457Leu
XM_005271322.2:c.1370A>T	XP_005271379.1:p.Gln457Leu
XM_005271323.2:c.1328A>T	XP_005271380.1:p.Gln443Leu
XM_005271324.3:c.1178A>T	XP_005271381.1:p.Gln393Leu
XM_005271325.2:c.1251+2462A>T	XP_005271382.1:n.1251+2462A>T
XM_005271326.2:c.1136A>T	XP_005271383.1:p.Gln379Leu
XM_005271327.2:c.953A>T	XP_005271384.1:p.Gln318Leu
XM_005271322.4:c.1370A>T	XP_005271379.1:p.Gln457Leu
XM_005271323.4:c.1328A>T	XP_005271380.1:p.Gln443Leu
XM_005271324.5:c.1178A>T	XP_005271381.1:p.Gln393Leu
XM_005271325.4:c.1251+2462A>T	XP_005271382.1:n.1251+2462A>T
XM_005271326.4:c.1136A>T	XP_005271383.1:p.Gln379Leu
XM_005271327.4:c.953A>T	XP_005271384.1:p.Gln318Leu
NM_001172309.2:c.1178A>T	NP_001165780.1:p.Gln393Leu
NM_144573.4:c.1370A>T MANE Select	NP_653174.3:p.Gln457Leu