Canonical Allele Identifier: CA185424

Gene: NEXN

Linked Data

• ClinVar Variation Id: 179916
• ClinVar RCV Id: RCV000156717
• dbSNP Id: rs727505219
• gnomAD v2: 1-78381782-T-C
• gnomAD v3: 1-77916097-T-C
• gnomAD v4: 1-77916097-T-C
• MyVariant Identifiers: chr1:g.78381782T>C (hg19) ; chr1:g.77916097T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77916097T>C , CM000663.2:g.77916097T>C	GRCh38
NC_000001.10:g.78381782T>C , CM000663.1:g.78381782T>C	GRCh37
NC_000001.9:g.78154370T>C	NCBI36
NG_016625.1:g.32583T>C , LRG_442:g.32583T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.-10T>C MANE Select	ENSP00000333938.7:n.-10T>C
ENST00000330010.12:c.-10T>C	ENSP00000327363.8:n.-10T>C
ENST00000334785.11:c.-10T>C	ENSP00000333938.7:n.-10T>C
ENST00000401035.7:c.-10T>C	ENSP00000383814.3:n.-10T>C
ENST00000440324.5:c.-10T>C	ENSP00000411902.1:n.-10T>C
NM_001172309.1:c.-10T>C	NP_001165780.1:n.-10T>C
NM_144573.3:c.-10T>C , LRG_442t1:c.-10T>C	NP_653174.3:n.-10T>C
XM_005271322.2:c.-10T>C	XP_005271379.1:n.-10T>C
XM_005271323.2:c.-10T>C	XP_005271380.1:n.-10T>C
XM_005271324.3:c.-10T>C	XP_005271381.1:n.-10T>C
XM_005271325.2:c.-10T>C	XP_005271382.1:n.-10T>C
XM_005271326.2:c.-10T>C	XP_005271383.1:n.-10T>C
XM_005271327.2:c.-10T>C	XP_005271384.1:n.-10T>C
XM_005271322.4:c.-10T>C	XP_005271379.1:n.-10T>C
XM_005271323.4:c.-10T>C	XP_005271380.1:n.-10T>C
XM_005271324.5:c.-10T>C	XP_005271381.1:n.-10T>C
XM_005271325.4:c.-10T>C	XP_005271382.1:n.-10T>C
XM_005271326.4:c.-10T>C	XP_005271383.1:n.-10T>C
XM_005271327.4:c.-10T>C	XP_005271384.1:n.-10T>C
NM_001172309.2:c.-10T>C	NP_001165780.1:n.-10T>C
NM_144573.4:c.-10T>C MANE Select	NP_653174.3:n.-10T>C