Canonical Allele Identifier: CA24692104

Gene: NEXN

Linked Data

• dbSNP Id: rs978824343
• MyVariant Identifiers: chr1:g.78408493T>C (hg19) ; chr1:g.77942808T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942808T>C , CM000663.2:g.77942808T>C	GRCh38
NC_000001.10:g.78408493T>C , CM000663.1:g.78408493T>C	GRCh37
NC_000001.9:g.78181081T>C	NCBI36
NG_016625.1:g.59294T>C , LRG_442:g.59294T>C
NG_033243.2:g.41286A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.2007T>C MANE Select	ENSP00000333938.7:p.Leu669=
ENST00000330010.12:c.1815T>C	ENSP00000327363.8:p.Leu605=
ENST00000334785.11:c.2007T>C	ENSP00000333938.7:p.Leu669=
ENST00000342754.5:c.1706T>C
ENST00000480732.2:n.1581T>C
NM_001172309.1:c.1815T>C	NP_001165780.1:p.Leu605=
NM_144573.3:c.2007T>C , LRG_442t1:c.2007T>C	NP_653174.3:p.Leu669=
XM_005271322.2:c.2007T>C	XP_005271379.1:p.Leu669=
XM_005271323.2:c.1965T>C	XP_005271380.1:p.Leu655=
XM_005271324.3:c.1815T>C	XP_005271381.1:p.Leu605=
XM_005271325.2:c.1785T>C	XP_005271382.1:p.Leu595=
XM_005271326.2:c.1773T>C	XP_005271383.1:p.Leu591=
XM_005271327.2:c.1590T>C	XP_005271384.1:p.Leu530=
XM_005271322.4:c.2007T>C	XP_005271379.1:p.Leu669=
XM_005271323.4:c.1965T>C	XP_005271380.1:p.Leu655=
XM_005271324.5:c.1815T>C	XP_005271381.1:p.Leu605=
XM_005271325.4:c.1785T>C	XP_005271382.1:p.Leu595=
XM_005271326.4:c.1773T>C	XP_005271383.1:p.Leu591=
XM_005271327.4:c.1590T>C	XP_005271384.1:p.Leu530=
NM_001172309.2:c.1815T>C	NP_001165780.1:p.Leu605=
NM_144573.4:c.2007T>C MANE Select	NP_653174.3:p.Leu669=