Canonical Allele Identifier: CA1177626893

Gene: NEXN

Linked Data

• dbSNP Id: rs910701913

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933577G>T , CM000663.2:g.77933577G>T	GRCh38
NC_000001.10:g.78399262G>T , CM000663.1:g.78399262G>T	GRCh37
NC_000001.9:g.78171850G>T	NCBI36
NG_016625.1:g.50063G>T , LRG_442:g.50063G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+98G>T MANE Select	ENSP00000333938.7:n.1251+98G>T
ENST00000330010.12:c.1059+98G>T	ENSP00000327363.8:n.1059+98G>T
ENST00000334785.11:c.1251+98G>T	ENSP00000333938.7:n.1251+98G>T
ENST00000342754.5:c.950+98G>T
ENST00000440324.5:c.1209+98G>T	ENSP00000411902.1:n.1209+98G>T
ENST00000464998.1:n.711+98G>T
ENST00000480732.2:n.825+98G>T
NM_001172309.1:c.1059+98G>T	NP_001165780.1:n.1059+98G>T
NM_144573.3:c.1251+98G>T , LRG_442t1:c.1251+98G>T	NP_653174.3:n.1251+98G>T
XM_005271322.2:c.1251+98G>T	XP_005271379.1:n.1251+98G>T
XM_005271323.2:c.1209+98G>T	XP_005271380.1:n.1209+98G>T
XM_005271324.3:c.1059+98G>T	XP_005271381.1:n.1059+98G>T
XM_005271325.2:c.1251+98G>T	XP_005271382.1:n.1251+98G>T
XM_005271326.2:c.1017+98G>T	XP_005271383.1:n.1017+98G>T
XM_005271327.2:c.834+98G>T	XP_005271384.1:n.834+98G>T
XM_005271322.4:c.1251+98G>T	XP_005271379.1:n.1251+98G>T
XM_005271323.4:c.1209+98G>T	XP_005271380.1:n.1209+98G>T
XM_005271324.5:c.1059+98G>T	XP_005271381.1:n.1059+98G>T
XM_005271325.4:c.1251+98G>T	XP_005271382.1:n.1251+98G>T
XM_005271326.4:c.1017+98G>T	XP_005271383.1:n.1017+98G>T
XM_005271327.4:c.834+98G>T	XP_005271384.1:n.834+98G>T
NM_001172309.2:c.1059+98G>T	NP_001165780.1:n.1059+98G>T
NM_144573.4:c.1251+98G>T MANE Select	NP_653174.3:n.1251+98G>T