Canonical Allele Identifier: CA918891

Gene: NEXN

Linked Data

• dbSNP Id: rs748737710
• ExAC: 1:78401766 G / C
• gnomAD v2: 1-78401766-G-C
• gnomAD v4: 1-77936081-G-C
• MyVariant Identifiers: chr1:g.78401766G>C (hg19) ; chr1:g.77936081G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936081G>C , CM000663.2:g.77936081G>C	GRCh38
NC_000001.10:g.78401766G>C , CM000663.1:g.78401766G>C	GRCh37
NC_000001.9:g.78174354G>C	NCBI36
NG_016625.1:g.52567G>C , LRG_442:g.52567G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+37G>C MANE Select	ENSP00000333938.7:n.1473+37G>C
ENST00000330010.12:c.1281+37G>C	ENSP00000327363.8:n.1281+37G>C
ENST00000334785.11:c.1473+37G>C	ENSP00000333938.7:n.1473+37G>C
ENST00000342754.5:c.1172+37G>C
ENST00000480732.2:n.1047+37G>C
NM_001172309.1:c.1281+37G>C	NP_001165780.1:n.1281+37G>C
NM_144573.3:c.1473+37G>C , LRG_442t1:c.1473+37G>C	NP_653174.3:n.1473+37G>C
XM_005271322.2:c.1473+37G>C	XP_005271379.1:n.1473+37G>C
XM_005271323.2:c.1431+37G>C	XP_005271380.1:n.1431+37G>C
XM_005271324.3:c.1281+37G>C	XP_005271381.1:n.1281+37G>C
XM_005271325.2:c.1251+2602G>C	XP_005271382.1:n.1251+2602G>C
XM_005271326.2:c.1239+37G>C	XP_005271383.1:n.1239+37G>C
XM_005271327.2:c.1056+37G>C	XP_005271384.1:n.1056+37G>C
XM_005271322.4:c.1473+37G>C	XP_005271379.1:n.1473+37G>C
XM_005271323.4:c.1431+37G>C	XP_005271380.1:n.1431+37G>C
XM_005271324.5:c.1281+37G>C	XP_005271381.1:n.1281+37G>C
XM_005271325.4:c.1251+2602G>C	XP_005271382.1:n.1251+2602G>C
XM_005271326.4:c.1239+37G>C	XP_005271383.1:n.1239+37G>C
XM_005271327.4:c.1056+37G>C	XP_005271384.1:n.1056+37G>C
NM_001172309.2:c.1281+37G>C	NP_001165780.1:n.1281+37G>C
NM_144573.4:c.1473+37G>C MANE Select	NP_653174.3:n.1473+37G>C