Canonical Allele Identifier: CA739060125

Gene: NEXN

Linked Data

• dbSNP Id: rs1249477902
• gnomAD v3: 1-77943064-C-G
• gnomAD v4: 1-77943064-C-G
• MyVariant Identifiers: chr1:g.78408749C>G (hg19) ; chr1:g.77943064C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943064C>G , CM000663.2:g.77943064C>G	GRCh38
NC_000001.10:g.78408749C>G , CM000663.1:g.78408749C>G	GRCh37
NC_000001.9:g.78181337C>G	NCBI36
NG_016625.1:g.59550C>G , LRG_442:g.59550C>G
NG_033243.2:g.41030G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*235C>G MANE Select	ENSP00000333938.7:n.*235C>G
ENST00000330010.12:c.*235C>G	ENSP00000327363.8:n.*235C>G
ENST00000334785.11:c.*235C>G	ENSP00000333938.7:n.*235C>G
ENST00000342754.5:c.1881C>G
ENST00000480732.2:n.1837C>G
NM_001172309.1:c.*235C>G	NP_001165780.1:n.*235C>G
NM_144573.3:c.*235C>G , LRG_442t1:c.*235C>G	NP_653174.3:n.*235C>G
XM_005271322.2:c.*151C>G	XP_005271379.1:n.*151C>G
XM_005271323.2:c.*151C>G	XP_005271380.1:n.*151C>G
XM_005271324.3:c.*151C>G	XP_005271381.1:n.*151C>G
XM_005271325.2:c.*151C>G	XP_005271382.1:n.*151C>G
XM_005271326.2:c.*151C>G	XP_005271383.1:n.*151C>G
XM_005271327.2:c.*151C>G	XP_005271384.1:n.*151C>G
XM_005271322.4:c.*151C>G	XP_005271379.1:n.*151C>G
XM_005271323.4:c.*151C>G	XP_005271380.1:n.*151C>G
XM_005271324.5:c.*151C>G	XP_005271381.1:n.*151C>G
XM_005271325.4:c.*151C>G	XP_005271382.1:n.*151C>G
XM_005271326.4:c.*151C>G	XP_005271383.1:n.*151C>G
XM_005271327.4:c.*151C>G	XP_005271384.1:n.*151C>G
NM_001172309.2:c.*235C>G	NP_001165780.1:n.*235C>G
NM_144573.4:c.*235C>G MANE Select	NP_653174.3:n.*235C>G