Canonical Allele Identifier: CA340878624

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401575G>C (hg19) ; chr1:g.77935890G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935890G>C , CM000663.2:g.77935890G>C	GRCh38
NC_000001.10:g.78401575G>C , CM000663.1:g.78401575G>C	GRCh37
NC_000001.9:g.78174163G>C	NCBI36
NG_016625.1:g.52376G>C , LRG_442:g.52376G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1319G>C MANE Select	ENSP00000333938.7:p.Ser440Thr
ENST00000330010.12:c.1127G>C	ENSP00000327363.8:p.Ser376Thr
ENST00000334785.11:c.1319G>C	ENSP00000333938.7:p.Ser440Thr
ENST00000342754.5:c.1018G>C
ENST00000440324.5:c.1277G>C	ENSP00000411902.1:p.Ser426Thr
ENST00000464998.1:n.779G>C
ENST00000480732.2:n.893G>C
NM_001172309.1:c.1127G>C	NP_001165780.1:p.Ser376Thr
NM_144573.3:c.1319G>C , LRG_442t1:c.1319G>C	NP_653174.3:p.Ser440Thr
XM_005271322.2:c.1319G>C	XP_005271379.1:p.Ser440Thr
XM_005271323.2:c.1277G>C	XP_005271380.1:p.Ser426Thr
XM_005271324.3:c.1127G>C	XP_005271381.1:p.Ser376Thr
XM_005271325.2:c.1251+2411G>C	XP_005271382.1:n.1251+2411G>C
XM_005271326.2:c.1085G>C	XP_005271383.1:p.Ser362Thr
XM_005271327.2:c.902G>C	XP_005271384.1:p.Ser301Thr
XM_005271322.4:c.1319G>C	XP_005271379.1:p.Ser440Thr
XM_005271323.4:c.1277G>C	XP_005271380.1:p.Ser426Thr
XM_005271324.5:c.1127G>C	XP_005271381.1:p.Ser376Thr
XM_005271325.4:c.1251+2411G>C	XP_005271382.1:n.1251+2411G>C
XM_005271326.4:c.1085G>C	XP_005271383.1:p.Ser362Thr
XM_005271327.4:c.902G>C	XP_005271384.1:p.Ser301Thr
NM_001172309.2:c.1127G>C	NP_001165780.1:p.Ser376Thr
NM_144573.4:c.1319G>C MANE Select	NP_653174.3:p.Ser440Thr