Canonical Allele Identifier: CA340876884

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78399060A>C (hg19) ; chr1:g.77933375A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933375A>C , CM000663.2:g.77933375A>C	GRCh38
NC_000001.10:g.78399060A>C , CM000663.1:g.78399060A>C	GRCh37
NC_000001.9:g.78171648A>C	NCBI36
NG_016625.1:g.49861A>C , LRG_442:g.49861A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1147A>C MANE Select	ENSP00000333938.7:p.Lys383Gln
ENST00000330010.12:c.955A>C	ENSP00000327363.8:p.Lys319Gln
ENST00000334785.11:c.1147A>C	ENSP00000333938.7:p.Lys383Gln
ENST00000342754.5:c.846A>C
ENST00000401035.7:c.955A>C	ENSP00000383814.3:p.Lys319Gln
ENST00000440324.5:c.1105A>C	ENSP00000411902.1:p.Lys369Gln
ENST00000464998.1:n.607A>C
ENST00000480732.2:n.721A>C
NM_001172309.1:c.955A>C	NP_001165780.1:p.Lys319Gln
NM_144573.3:c.1147A>C , LRG_442t1:c.1147A>C	NP_653174.3:p.Lys383Gln
XM_005271322.2:c.1147A>C	XP_005271379.1:p.Lys383Gln
XM_005271323.2:c.1105A>C	XP_005271380.1:p.Lys369Gln
XM_005271324.3:c.955A>C	XP_005271381.1:p.Lys319Gln
XM_005271325.2:c.1147A>C	XP_005271382.1:p.Lys383Gln
XM_005271326.2:c.913A>C	XP_005271383.1:p.Lys305Gln
XM_005271327.2:c.730A>C	XP_005271384.1:p.Lys244Gln
XM_005271322.4:c.1147A>C	XP_005271379.1:p.Lys383Gln
XM_005271323.4:c.1105A>C	XP_005271380.1:p.Lys369Gln
XM_005271324.5:c.955A>C	XP_005271381.1:p.Lys319Gln
XM_005271325.4:c.1147A>C	XP_005271382.1:p.Lys383Gln
XM_005271326.4:c.913A>C	XP_005271383.1:p.Lys305Gln
XM_005271327.4:c.730A>C	XP_005271384.1:p.Lys244Gln
NM_001172309.2:c.955A>C	NP_001165780.1:p.Lys319Gln
NM_144573.4:c.1147A>C MANE Select	NP_653174.3:p.Lys383Gln