Canonical Allele Identifier: CA340883723

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408487T>G (hg19) ; chr1:g.77942802T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942802T>G , CM000663.2:g.77942802T>G	GRCh38
NC_000001.10:g.78408487T>G , CM000663.1:g.78408487T>G	GRCh37
NC_000001.9:g.78181075T>G	NCBI36
NG_016625.1:g.59288T>G , LRG_442:g.59288T>G
NG_033243.2:g.41292A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.2001T>G MANE Select	ENSP00000333938.7:p.Cys667Trp
ENST00000330010.12:c.1809T>G	ENSP00000327363.8:p.Cys603Trp
ENST00000334785.11:c.2001T>G	ENSP00000333938.7:p.Cys667Trp
ENST00000342754.5:c.1700T>G
ENST00000480732.2:n.1575T>G
NM_001172309.1:c.1809T>G	NP_001165780.1:p.Cys603Trp
NM_144573.3:c.2001T>G , LRG_442t1:c.2001T>G	NP_653174.3:p.Cys667Trp
XM_005271322.2:c.2001T>G	XP_005271379.1:p.Cys667Trp
XM_005271323.2:c.1959T>G	XP_005271380.1:p.Cys653Trp
XM_005271324.3:c.1809T>G	XP_005271381.1:p.Cys603Trp
XM_005271325.2:c.1779T>G	XP_005271382.1:p.Cys593Trp
XM_005271326.2:c.1767T>G	XP_005271383.1:p.Cys589Trp
XM_005271327.2:c.1584T>G	XP_005271384.1:p.Cys528Trp
XM_005271322.4:c.2001T>G	XP_005271379.1:p.Cys667Trp
XM_005271323.4:c.1959T>G	XP_005271380.1:p.Cys653Trp
XM_005271324.5:c.1809T>G	XP_005271381.1:p.Cys603Trp
XM_005271325.4:c.1779T>G	XP_005271382.1:p.Cys593Trp
XM_005271326.4:c.1767T>G	XP_005271383.1:p.Cys589Trp
XM_005271327.4:c.1584T>G	XP_005271384.1:p.Cys528Trp
NM_001172309.2:c.1809T>G	NP_001165780.1:p.Cys603Trp
NM_144573.4:c.2001T>G MANE Select	NP_653174.3:p.Cys667Trp