Canonical Allele Identifier: CA340880935

Gene: NEXN

Linked Data

• dbSNP Id: rs2102177211
• MyVariant Identifiers: chr1:g.78407773G>A (hg19) ; chr1:g.77942088G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942088G>A , CM000663.2:g.77942088G>A	GRCh38
NC_000001.10:g.78407773G>A , CM000663.1:g.78407773G>A	GRCh37
NC_000001.9:g.78180361G>A	NCBI36
NG_016625.1:g.58574G>A , LRG_442:g.58574G>A
NG_033243.2:g.42006C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1539G>A MANE Select	ENSP00000333938.7:p.Met513Ile
ENST00000330010.12:c.1347G>A	ENSP00000327363.8:p.Met449Ile
ENST00000334785.11:c.1539G>A	ENSP00000333938.7:p.Met513Ile
ENST00000342754.5:c.1238G>A
ENST00000470735.1:n.378G>A
ENST00000480732.2:n.1113G>A
NM_001172309.1:c.1347G>A	NP_001165780.1:p.Met449Ile
NM_144573.3:c.1539G>A , LRG_442t1:c.1539G>A	NP_653174.3:p.Met513Ile
XM_005271322.2:c.1539G>A	XP_005271379.1:p.Met513Ile
XM_005271323.2:c.1497G>A	XP_005271380.1:p.Met499Ile
XM_005271324.3:c.1347G>A	XP_005271381.1:p.Met449Ile
XM_005271325.2:c.1317G>A	XP_005271382.1:p.Met439Ile
XM_005271326.2:c.1305G>A	XP_005271383.1:p.Met435Ile
XM_005271327.2:c.1122G>A	XP_005271384.1:p.Met374Ile
XM_005271322.4:c.1539G>A	XP_005271379.1:p.Met513Ile
XM_005271323.4:c.1497G>A	XP_005271380.1:p.Met499Ile
XM_005271324.5:c.1347G>A	XP_005271381.1:p.Met449Ile
XM_005271325.4:c.1317G>A	XP_005271382.1:p.Met439Ile
XM_005271326.4:c.1305G>A	XP_005271383.1:p.Met435Ile
XM_005271327.4:c.1122G>A	XP_005271384.1:p.Met374Ile
NM_001172309.2:c.1347G>A	NP_001165780.1:p.Met449Ile
NM_144573.4:c.1539G>A MANE Select	NP_653174.3:p.Met513Ile