Canonical Allele Identifier: CA418574038

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408472T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942787T>A , CM000663.2:g.77942787T>A	GRCh38
NC_000001.10:g.78408472T>A , CM000663.1:g.78408472T>A	GRCh37
NC_000001.9:g.78181060T>A	NCBI36
NG_016625.1:g.59273T>A , LRG_442:g.59273T>A
NG_033243.2:g.41307A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1986T>A MANE Select	ENSP00000333938.7:p.Ser662=
ENST00000330010.12:c.1794T>A	ENSP00000327363.8:p.Ser598=
ENST00000334785.11:c.1986T>A	ENSP00000333938.7:p.Ser662=
ENST00000342754.5:c.1685T>A
ENST00000480732.2:n.1560T>A
NM_001172309.1:c.1794T>A	NP_001165780.1:p.Ser598=
NM_144573.3:c.1986T>A , LRG_442t1:c.1986T>A	NP_653174.3:p.Ser662=
XM_005271322.2:c.1986T>A	XP_005271379.1:p.Ser662=
XM_005271323.2:c.1944T>A	XP_005271380.1:p.Ser648=
XM_005271324.3:c.1794T>A	XP_005271381.1:p.Ser598=
XM_005271325.2:c.1764T>A	XP_005271382.1:p.Ser588=
XM_005271326.2:c.1752T>A	XP_005271383.1:p.Ser584=
XM_005271327.2:c.1569T>A	XP_005271384.1:p.Ser523=
XM_005271322.4:c.1986T>A	XP_005271379.1:p.Ser662=
XM_005271323.4:c.1944T>A	XP_005271380.1:p.Ser648=
XM_005271324.5:c.1794T>A	XP_005271381.1:p.Ser598=
XM_005271325.4:c.1764T>A	XP_005271382.1:p.Ser588=
XM_005271326.4:c.1752T>A	XP_005271383.1:p.Ser584=
XM_005271327.4:c.1569T>A	XP_005271384.1:p.Ser523=
NM_001172309.2:c.1794T>A	NP_001165780.1:p.Ser598=
NM_144573.4:c.1986T>A MANE Select	NP_653174.3:p.Ser662=