Canonical Allele Identifier: CA340881046

Gene: NEXN

Linked Data

• dbSNP Id: rs1651371056
• MyVariant Identifiers: chr1:g.78407793T>C (hg19) ; chr1:g.77942108T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942108T>C , CM000663.2:g.77942108T>C	GRCh38
NC_000001.10:g.78407793T>C , CM000663.1:g.78407793T>C	GRCh37
NC_000001.9:g.78180381T>C	NCBI36
NG_016625.1:g.58594T>C , LRG_442:g.58594T>C
NG_033243.2:g.41986A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1559T>C MANE Select	ENSP00000333938.7:p.Met520Thr
ENST00000330010.12:c.1367T>C	ENSP00000327363.8:p.Met456Thr
ENST00000334785.11:c.1559T>C	ENSP00000333938.7:p.Met520Thr
ENST00000342754.5:c.1258T>C
ENST00000470735.1:n.398T>C
ENST00000480732.2:n.1133T>C
NM_001172309.1:c.1367T>C	NP_001165780.1:p.Met456Thr
NM_144573.3:c.1559T>C , LRG_442t1:c.1559T>C	NP_653174.3:p.Met520Thr
XM_005271322.2:c.1559T>C	XP_005271379.1:p.Met520Thr
XM_005271323.2:c.1517T>C	XP_005271380.1:p.Met506Thr
XM_005271324.3:c.1367T>C	XP_005271381.1:p.Met456Thr
XM_005271325.2:c.1337T>C	XP_005271382.1:p.Met446Thr
XM_005271326.2:c.1325T>C	XP_005271383.1:p.Met442Thr
XM_005271327.2:c.1142T>C	XP_005271384.1:p.Met381Thr
XM_005271322.4:c.1559T>C	XP_005271379.1:p.Met520Thr
XM_005271323.4:c.1517T>C	XP_005271380.1:p.Met506Thr
XM_005271324.5:c.1367T>C	XP_005271381.1:p.Met456Thr
XM_005271325.4:c.1337T>C	XP_005271382.1:p.Met446Thr
XM_005271326.4:c.1325T>C	XP_005271383.1:p.Met442Thr
XM_005271327.4:c.1142T>C	XP_005271384.1:p.Met381Thr
NM_001172309.2:c.1367T>C	NP_001165780.1:p.Met456Thr
NM_144573.4:c.1559T>C MANE Select	NP_653174.3:p.Met520Thr