Canonical Allele Identifier: CA340883172

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408397C>G (hg19) ; chr1:g.77942712C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942712C>G , CM000663.2:g.77942712C>G	GRCh38
NC_000001.10:g.78408397C>G , CM000663.1:g.78408397C>G	GRCh37
NC_000001.9:g.78180985C>G	NCBI36
NG_016625.1:g.59198C>G , LRG_442:g.59198C>G
NG_033243.2:g.41382G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1911C>G MANE Select	ENSP00000333938.7:p.Tyr637Ter
ENST00000330010.12:c.1719C>G	ENSP00000327363.8:p.Tyr573Ter
ENST00000334785.11:c.1911C>G	ENSP00000333938.7:p.Tyr637Ter
ENST00000342754.5:c.1610C>G
ENST00000470735.1:n.750C>G
ENST00000480732.2:n.1485C>G
NM_001172309.1:c.1719C>G	NP_001165780.1:p.Tyr573Ter
NM_144573.3:c.1911C>G , LRG_442t1:c.1911C>G	NP_653174.3:p.Tyr637Ter
XM_005271322.2:c.1911C>G	XP_005271379.1:p.Tyr637Ter
XM_005271323.2:c.1869C>G	XP_005271380.1:p.Tyr623Ter
XM_005271324.3:c.1719C>G	XP_005271381.1:p.Tyr573Ter
XM_005271325.2:c.1689C>G	XP_005271382.1:p.Tyr563Ter
XM_005271326.2:c.1677C>G	XP_005271383.1:p.Tyr559Ter
XM_005271327.2:c.1494C>G	XP_005271384.1:p.Tyr498Ter
XM_005271322.4:c.1911C>G	XP_005271379.1:p.Tyr637Ter
XM_005271323.4:c.1869C>G	XP_005271380.1:p.Tyr623Ter
XM_005271324.5:c.1719C>G	XP_005271381.1:p.Tyr573Ter
XM_005271325.4:c.1689C>G	XP_005271382.1:p.Tyr563Ter
XM_005271326.4:c.1677C>G	XP_005271383.1:p.Tyr559Ter
XM_005271327.4:c.1494C>G	XP_005271384.1:p.Tyr498Ter
NM_001172309.2:c.1719C>G	NP_001165780.1:p.Tyr573Ter
NM_144573.4:c.1911C>G MANE Select	NP_653174.3:p.Tyr637Ter