Canonical Allele Identifier: CA076791

Gene: NEXN

Linked Data

• ClinVar Variation Id: 222753
• ClinVar RCV Id: RCV000208073 ; RCV000248087
• dbSNP Id: rs370195451
• ExAC: 1:78401656 T / C
• gnomAD v2: 1-78401656-T-C
• gnomAD v3: 1-77935971-T-C
• gnomAD v4: 1-77935971-T-C
• MyVariant Identifiers: chr1:g.78401656T>C (hg19) ; chr1:g.78401656_78401659delinsCAGA (hg19) ; chr1:g.77935971T>C (hg38) ; chr1:g.77935971_77935974delinsCAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935971T>C , CM000663.2:g.77935971T>C	GRCh38
NC_000001.10:g.78401656T>C , CM000663.1:g.78401656T>C	GRCh37
NC_000001.9:g.78174244T>C	NCBI36
NG_016625.1:g.52457T>C , LRG_442:g.52457T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1400T>C MANE Select	ENSP00000333938.7:p.Ile467Thr
ENST00000330010.12:c.1208T>C	ENSP00000327363.8:p.Ile403Thr
ENST00000334785.11:c.1400T>C	ENSP00000333938.7:p.Ile467Thr
ENST00000342754.5:c.1099T>C
ENST00000480732.2:n.974T>C
NM_001172309.1:c.1208T>C	NP_001165780.1:p.Ile403Thr
NM_144573.3:c.1400T>C , LRG_442t1:c.1400T>C	NP_653174.3:p.Ile467Thr
XM_005271322.2:c.1400T>C	XP_005271379.1:p.Ile467Thr
XM_005271323.2:c.1358T>C	XP_005271380.1:p.Ile453Thr
XM_005271324.3:c.1208T>C	XP_005271381.1:p.Ile403Thr
XM_005271325.2:c.1251+2492T>C	XP_005271382.1:n.1251+2492T>C
XM_005271326.2:c.1166T>C	XP_005271383.1:p.Ile389Thr
XM_005271327.2:c.983T>C	XP_005271384.1:p.Ile328Thr
XM_005271322.4:c.1400T>C	XP_005271379.1:p.Ile467Thr
XM_005271323.4:c.1358T>C	XP_005271380.1:p.Ile453Thr
XM_005271324.5:c.1208T>C	XP_005271381.1:p.Ile403Thr
XM_005271325.4:c.1251+2492T>C	XP_005271382.1:n.1251+2492T>C
XM_005271326.4:c.1166T>C	XP_005271383.1:p.Ile389Thr
XM_005271327.4:c.983T>C	XP_005271384.1:p.Ile328Thr
NM_001172309.2:c.1208T>C	NP_001165780.1:p.Ile403Thr
NM_144573.4:c.1400T>C MANE Select	NP_653174.3:p.Ile467Thr