Canonical Allele Identifier: CA340883279

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408445G>T (hg19) ; chr1:g.77942760G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942760G>T , CM000663.2:g.77942760G>T	GRCh38
NC_000001.10:g.78408445G>T , CM000663.1:g.78408445G>T	GRCh37
NC_000001.9:g.78181033G>T	NCBI36
NG_016625.1:g.59246G>T , LRG_442:g.59246G>T
NG_033243.2:g.41334C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1959G>T MANE Select	ENSP00000333938.7:p.Met653Ile
ENST00000330010.12:c.1767G>T	ENSP00000327363.8:p.Met589Ile
ENST00000334785.11:c.1959G>T	ENSP00000333938.7:p.Met653Ile
ENST00000342754.5:c.1658G>T
ENST00000480732.2:n.1533G>T
NM_001172309.1:c.1767G>T	NP_001165780.1:p.Met589Ile
NM_144573.3:c.1959G>T , LRG_442t1:c.1959G>T	NP_653174.3:p.Met653Ile
XM_005271322.2:c.1959G>T	XP_005271379.1:p.Met653Ile
XM_005271323.2:c.1917G>T	XP_005271380.1:p.Met639Ile
XM_005271324.3:c.1767G>T	XP_005271381.1:p.Met589Ile
XM_005271325.2:c.1737G>T	XP_005271382.1:p.Met579Ile
XM_005271326.2:c.1725G>T	XP_005271383.1:p.Met575Ile
XM_005271327.2:c.1542G>T	XP_005271384.1:p.Met514Ile
XM_005271322.4:c.1959G>T	XP_005271379.1:p.Met653Ile
XM_005271323.4:c.1917G>T	XP_005271380.1:p.Met639Ile
XM_005271324.5:c.1767G>T	XP_005271381.1:p.Met589Ile
XM_005271325.4:c.1737G>T	XP_005271382.1:p.Met579Ile
XM_005271326.4:c.1725G>T	XP_005271383.1:p.Met575Ile
XM_005271327.4:c.1542G>T	XP_005271384.1:p.Met514Ile
NM_001172309.2:c.1767G>T	NP_001165780.1:p.Met589Ile
NM_144573.4:c.1959G>T MANE Select	NP_653174.3:p.Met653Ile