Canonical Allele Identifier: CA2739708130

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942909A>C , CM000663.2:g.77942909A>C	GRCh38
NC_000001.10:g.78408594A>C , CM000663.1:g.78408594A>C	GRCh37
NC_000001.9:g.78181182A>C	NCBI36
NG_016625.1:g.59395A>C , LRG_442:g.59395A>C
NG_033243.2:g.41185T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*80A>C MANE Select	ENSP00000333938.7:n.*80A>C
ENST00000330010.12:c.*80A>C	ENSP00000327363.8:n.*80A>C
ENST00000334785.11:c.*80A>C	ENSP00000333938.7:n.*80A>C
ENST00000342754.5:c.1726A>C
ENST00000480732.2:n.1682A>C
NM_001172309.1:c.*80A>C	NP_001165780.1:n.*80A>C
NM_144573.3:c.*80A>C , LRG_442t1:c.*80A>C	NP_653174.3:n.*80A>C
XM_005271322.2:c.2027A>C	XP_005271379.1:p.Tyr676Ser
XM_005271323.2:c.1985A>C	XP_005271380.1:p.Tyr662Ser
XM_005271324.3:c.1835A>C	XP_005271381.1:p.Tyr612Ser
XM_005271325.2:c.1805A>C	XP_005271382.1:p.Tyr602Ser
XM_005271326.2:c.1793A>C	XP_005271383.1:p.Tyr598Ser
XM_005271327.2:c.1610A>C	XP_005271384.1:p.Tyr537Ser
XM_005271322.4:c.2027A>C	XP_005271379.1:p.Tyr676Ser
XM_005271323.4:c.1985A>C	XP_005271380.1:p.Tyr662Ser
XM_005271324.5:c.1835A>C	XP_005271381.1:p.Tyr612Ser
XM_005271325.4:c.1805A>C	XP_005271382.1:p.Tyr602Ser
XM_005271326.4:c.1793A>C	XP_005271383.1:p.Tyr598Ser
XM_005271327.4:c.1610A>C	XP_005271384.1:p.Tyr537Ser
NM_001172309.2:c.*80A>C	NP_001165780.1:n.*80A>C
NM_144573.4:c.*80A>C MANE Select	NP_653174.3:n.*80A>C