Canonical Allele Identifier: CA340883081

Gene: NEXN

Linked Data

• dbSNP Id: rs1202499982
• gnomAD v2: 1-78408357-A-G
• gnomAD v4: 1-77942672-A-G
• MyVariant Identifiers: chr1:g.78408357A>G (hg19) ; chr1:g.77942672A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942672A>G , CM000663.2:g.77942672A>G	GRCh38
NC_000001.10:g.78408357A>G , CM000663.1:g.78408357A>G	GRCh37
NC_000001.9:g.78180945A>G	NCBI36
NG_016625.1:g.59158A>G , LRG_442:g.59158A>G
NG_033243.2:g.41422T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1871A>G MANE Select	ENSP00000333938.7:p.Asp624Gly
ENST00000330010.12:c.1679A>G	ENSP00000327363.8:p.Asp560Gly
ENST00000334785.11:c.1871A>G	ENSP00000333938.7:p.Asp624Gly
ENST00000342754.5:c.1570A>G
ENST00000470735.1:n.710A>G
ENST00000480732.2:n.1445A>G
NM_001172309.1:c.1679A>G	NP_001165780.1:p.Asp560Gly
NM_144573.3:c.1871A>G , LRG_442t1:c.1871A>G	NP_653174.3:p.Asp624Gly
XM_005271322.2:c.1871A>G	XP_005271379.1:p.Asp624Gly
XM_005271323.2:c.1829A>G	XP_005271380.1:p.Asp610Gly
XM_005271324.3:c.1679A>G	XP_005271381.1:p.Asp560Gly
XM_005271325.2:c.1649A>G	XP_005271382.1:p.Asp550Gly
XM_005271326.2:c.1637A>G	XP_005271383.1:p.Asp546Gly
XM_005271327.2:c.1454A>G	XP_005271384.1:p.Asp485Gly
XM_005271322.4:c.1871A>G	XP_005271379.1:p.Asp624Gly
XM_005271323.4:c.1829A>G	XP_005271380.1:p.Asp610Gly
XM_005271324.5:c.1679A>G	XP_005271381.1:p.Asp560Gly
XM_005271325.4:c.1649A>G	XP_005271382.1:p.Asp550Gly
XM_005271326.4:c.1637A>G	XP_005271383.1:p.Asp546Gly
XM_005271327.4:c.1454A>G	XP_005271384.1:p.Asp485Gly
NM_001172309.2:c.1679A>G	NP_001165780.1:p.Asp560Gly
NM_144573.4:c.1871A>G MANE Select	NP_653174.3:p.Asp624Gly