Canonical Allele Identifier: CA340873984

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926789T>C , CM000663.2:g.77926789T>C	GRCh38
NC_000001.10:g.78392474T>C , CM000663.1:g.78392474T>C	GRCh37
NC_000001.9:g.78165062T>C	NCBI36
NG_016625.1:g.43275T>C , LRG_442:g.43275T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144573.4:c.761T>C MANE Select	NP_653174.3:p.Leu254Pro
ENST00000334785.12:c.761T>C MANE Select	ENSP00000333938.7:p.Leu254Pro
NM_001172309.1:c.569T>C	NP_001165780.1:p.Leu190Pro
NM_001172309.2:c.569T>C	NP_001165780.1:p.Leu190Pro
NM_144573.3:c.761T>C , LRG_442t1:c.761T>C	NP_653174.3:p.Leu254Pro
ENST00000330010.12:c.569T>C	ENSP00000327363.8:p.Leu190Pro
ENST00000334785.11:c.761T>C	ENSP00000333938.7:p.Leu254Pro
ENST00000342754.5:c.460T>C
ENST00000401035.7:c.569T>C	ENSP00000383814.3:p.Leu190Pro
ENST00000440324.5:c.719T>C	ENSP00000411902.1:p.Leu240Pro
ENST00000464998.1:n.221T>C
XM_005271322.2:c.761T>C	XP_005271379.1:p.Leu254Pro
XM_005271322.4:c.761T>C	XP_005271379.1:p.Leu254Pro
XM_005271323.2:c.719T>C	XP_005271380.1:p.Leu240Pro
XM_005271323.4:c.719T>C	XP_005271380.1:p.Leu240Pro
XM_005271324.3:c.569T>C	XP_005271381.1:p.Leu190Pro
XM_005271324.5:c.569T>C	XP_005271381.1:p.Leu190Pro
XM_005271325.2:c.761T>C	XP_005271382.1:p.Leu254Pro
XM_005271325.4:c.761T>C	XP_005271382.1:p.Leu254Pro
XM_005271326.2:c.527T>C	XP_005271383.1:p.Leu176Pro
XM_005271326.4:c.527T>C	XP_005271383.1:p.Leu176Pro
XM_005271327.2:c.448-2527T>C	XP_005271384.1:n.448-2527T>C
XM_005271327.4:c.448-2527T>C	XP_005271384.1:n.448-2527T>C