Canonical Allele Identifier: CA340883349

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408467G>C (hg19) ; chr1:g.77942782G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942782G>C , CM000663.2:g.77942782G>C	GRCh38
NC_000001.10:g.78408467G>C , CM000663.1:g.78408467G>C	GRCh37
NC_000001.9:g.78181055G>C	NCBI36
NG_016625.1:g.59268G>C , LRG_442:g.59268G>C
NG_033243.2:g.41312C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1981G>C MANE Select	ENSP00000333938.7:p.Gly661Arg
ENST00000330010.12:c.1789G>C	ENSP00000327363.8:p.Gly597Arg
ENST00000334785.11:c.1981G>C	ENSP00000333938.7:p.Gly661Arg
ENST00000342754.5:c.1680G>C
ENST00000480732.2:n.1555G>C
NM_001172309.1:c.1789G>C	NP_001165780.1:p.Gly597Arg
NM_144573.3:c.1981G>C , LRG_442t1:c.1981G>C	NP_653174.3:p.Gly661Arg
XM_005271322.2:c.1981G>C	XP_005271379.1:p.Gly661Arg
XM_005271323.2:c.1939G>C	XP_005271380.1:p.Gly647Arg
XM_005271324.3:c.1789G>C	XP_005271381.1:p.Gly597Arg
XM_005271325.2:c.1759G>C	XP_005271382.1:p.Gly587Arg
XM_005271326.2:c.1747G>C	XP_005271383.1:p.Gly583Arg
XM_005271327.2:c.1564G>C	XP_005271384.1:p.Gly522Arg
XM_005271322.4:c.1981G>C	XP_005271379.1:p.Gly661Arg
XM_005271323.4:c.1939G>C	XP_005271380.1:p.Gly647Arg
XM_005271324.5:c.1789G>C	XP_005271381.1:p.Gly597Arg
XM_005271325.4:c.1759G>C	XP_005271382.1:p.Gly587Arg
XM_005271326.4:c.1747G>C	XP_005271383.1:p.Gly583Arg
XM_005271327.4:c.1564G>C	XP_005271384.1:p.Gly522Arg
NM_001172309.2:c.1789G>C	NP_001165780.1:p.Gly597Arg
NM_144573.4:c.1981G>C MANE Select	NP_653174.3:p.Gly661Arg