Canonical Allele Identifier: CA918805

Gene: NEXN

Linked Data

• dbSNP Id: rs544770390
• ExAC: 1:78399023 A / T
• gnomAD v2: 1-78399023-A-T
• gnomAD v3: 1-77933338-A-T
• gnomAD v4: 1-77933338-A-T
• MyVariant Identifiers: chr1:g.78399023A>T (hg19) ; chr1:g.77933338A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933338A>T , CM000663.2:g.77933338A>T	GRCh38
NC_000001.10:g.78399023A>T , CM000663.1:g.78399023A>T	GRCh37
NC_000001.9:g.78171611A>T	NCBI36
NG_016625.1:g.49824A>T , LRG_442:g.49824A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1110A>T MANE Select	ENSP00000333938.7:p.Thr370=
ENST00000330010.12:c.918A>T	ENSP00000327363.8:p.Thr306=
ENST00000334785.11:c.1110A>T	ENSP00000333938.7:p.Thr370=
ENST00000342754.5:c.809A>T
ENST00000401035.7:c.918A>T	ENSP00000383814.3:p.Thr306=
ENST00000440324.5:c.1068A>T	ENSP00000411902.1:p.Thr356=
ENST00000464998.1:n.570A>T
ENST00000480732.2:n.684A>T
NM_001172309.1:c.918A>T	NP_001165780.1:p.Thr306=
NM_144573.3:c.1110A>T , LRG_442t1:c.1110A>T	NP_653174.3:p.Thr370=
XM_005271322.2:c.1110A>T	XP_005271379.1:p.Thr370=
XM_005271323.2:c.1068A>T	XP_005271380.1:p.Thr356=
XM_005271324.3:c.918A>T	XP_005271381.1:p.Thr306=
XM_005271325.2:c.1110A>T	XP_005271382.1:p.Thr370=
XM_005271326.2:c.876A>T	XP_005271383.1:p.Thr292=
XM_005271327.2:c.693A>T	XP_005271384.1:p.Thr231=
XM_005271322.4:c.1110A>T	XP_005271379.1:p.Thr370=
XM_005271323.4:c.1068A>T	XP_005271380.1:p.Thr356=
XM_005271324.5:c.918A>T	XP_005271381.1:p.Thr306=
XM_005271325.4:c.1110A>T	XP_005271382.1:p.Thr370=
XM_005271326.4:c.876A>T	XP_005271383.1:p.Thr292=
XM_005271327.4:c.693A>T	XP_005271384.1:p.Thr231=
NM_001172309.2:c.918A>T	NP_001165780.1:p.Thr306=
NM_144573.4:c.1110A>T MANE Select	NP_653174.3:p.Thr370=