Canonical Allele Identifier: CA2744247094

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943091T>A , CM000663.2:g.77943091T>A	GRCh38
NC_000001.10:g.78408776T>A , CM000663.1:g.78408776T>A	GRCh37
NC_000001.9:g.78181364T>A	NCBI36
NG_016625.1:g.59577T>A , LRG_442:g.59577T>A
NG_033243.2:g.41003A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*262T>A MANE Select	ENSP00000333938.7:n.*262T>A
ENST00000330010.12:c.*262T>A	ENSP00000327363.8:n.*262T>A
ENST00000334785.11:c.*262T>A	ENSP00000333938.7:n.*262T>A
ENST00000342754.5:c.1908T>A
ENST00000480732.2:n.1864T>A
NM_001172309.1:c.*262T>A	NP_001165780.1:n.*262T>A
NM_144573.3:c.*262T>A , LRG_442t1:c.*262T>A	NP_653174.3:n.*262T>A
XM_005271322.2:c.*178T>A	XP_005271379.1:n.*178T>A
XM_005271323.2:c.*178T>A	XP_005271380.1:n.*178T>A
XM_005271324.3:c.*178T>A	XP_005271381.1:n.*178T>A
XM_005271325.2:c.*178T>A	XP_005271382.1:n.*178T>A
XM_005271326.2:c.*178T>A	XP_005271383.1:n.*178T>A
XM_005271327.2:c.*178T>A	XP_005271384.1:n.*178T>A
XM_005271322.4:c.*178T>A	XP_005271379.1:n.*178T>A
XM_005271323.4:c.*178T>A	XP_005271380.1:n.*178T>A
XM_005271324.5:c.*178T>A	XP_005271381.1:n.*178T>A
XM_005271325.4:c.*178T>A	XP_005271382.1:n.*178T>A
XM_005271326.4:c.*178T>A	XP_005271383.1:n.*178T>A
XM_005271327.4:c.*178T>A	XP_005271384.1:n.*178T>A
NM_001172309.2:c.*262T>A	NP_001165780.1:n.*262T>A
NM_144573.4:c.*262T>A MANE Select	NP_653174.3:n.*262T>A