Canonical Allele Identifier: CA523842815

Gene: NEXN

Linked Data

• dbSNP Id: rs1287810607
• gnomAD v2: 1-78408589-T-C
• gnomAD v3: 1-77942904-T-C
• gnomAD v4: 1-77942904-T-C
• MyVariant Identifiers: chr1:g.78408589T>C (hg19) ; chr1:g.77942904T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942904T>C , CM000663.2:g.77942904T>C	GRCh38
NC_000001.10:g.78408589T>C , CM000663.1:g.78408589T>C	GRCh37
NC_000001.9:g.78181177T>C	NCBI36
NG_016625.1:g.59390T>C , LRG_442:g.59390T>C
NG_033243.2:g.41190A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*75T>C MANE Select	ENSP00000333938.7:n.*75T>C
ENST00000330010.12:c.*75T>C	ENSP00000327363.8:n.*75T>C
ENST00000334785.11:c.*75T>C	ENSP00000333938.7:n.*75T>C
ENST00000342754.5:c.1721T>C
ENST00000480732.2:n.1677T>C
NM_001172309.1:c.*75T>C	NP_001165780.1:n.*75T>C
NM_144573.3:c.*75T>C , LRG_442t1:c.*75T>C	NP_653174.3:n.*75T>C
XM_005271322.2:c.2022T>C	XP_005271379.1:p.Asp674=
XM_005271323.2:c.1980T>C	XP_005271380.1:p.Asp660=
XM_005271324.3:c.1830T>C	XP_005271381.1:p.Asp610=
XM_005271325.2:c.1800T>C	XP_005271382.1:p.Asp600=
XM_005271326.2:c.1788T>C	XP_005271383.1:p.Asp596=
XM_005271327.2:c.1605T>C	XP_005271384.1:p.Asp535=
XM_005271322.4:c.2022T>C	XP_005271379.1:p.Asp674=
XM_005271323.4:c.1980T>C	XP_005271380.1:p.Asp660=
XM_005271324.5:c.1830T>C	XP_005271381.1:p.Asp610=
XM_005271325.4:c.1800T>C	XP_005271382.1:p.Asp600=
XM_005271326.4:c.1788T>C	XP_005271383.1:p.Asp596=
XM_005271327.4:c.1605T>C	XP_005271384.1:p.Asp535=
NM_001172309.2:c.*75T>C	NP_001165780.1:n.*75T>C
NM_144573.4:c.*75T>C MANE Select	NP_653174.3:n.*75T>C