Canonical Allele Identifier: CA418709556

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942640T>C , CM000663.2:g.77942640T>C	GRCh38
NC_000001.10:g.78408325T>C , CM000663.1:g.78408325T>C	GRCh37
NC_000001.9:g.78180913T>C	NCBI36
NG_016625.1:g.59126T>C , LRG_442:g.59126T>C
NG_033243.2:g.41454A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_144573.4:c.1839T>C MANE Select	NP_653174.3:p.Ile613=
ENST00000334785.12:c.1839T>C MANE Select	ENSP00000333938.7:p.Ile613=
NM_001172309.1:c.1647T>C	NP_001165780.1:p.Ile549=
NM_001172309.2:c.1647T>C	NP_001165780.1:p.Ile549=
NM_144573.3:c.1839T>C , LRG_442t1:c.1839T>C	NP_653174.3:p.Ile613=
ENST00000330010.12:c.1647T>C	ENSP00000327363.8:p.Ile549=
ENST00000334785.11:c.1839T>C	ENSP00000333938.7:p.Ile613=
ENST00000342754.5:c.1538T>C
ENST00000470735.1:n.678T>C
ENST00000480732.2:n.1413T>C
XM_005271322.2:c.1839T>C	XP_005271379.1:p.Ile613=
XM_005271322.4:c.1839T>C	XP_005271379.1:p.Ile613=
XM_005271323.2:c.1797T>C	XP_005271380.1:p.Ile599=
XM_005271323.4:c.1797T>C	XP_005271380.1:p.Ile599=
XM_005271324.3:c.1647T>C	XP_005271381.1:p.Ile549=
XM_005271324.5:c.1647T>C	XP_005271381.1:p.Ile549=
XM_005271325.2:c.1617T>C	XP_005271382.1:p.Ile539=
XM_005271325.4:c.1617T>C	XP_005271382.1:p.Ile539=
XM_005271326.2:c.1605T>C	XP_005271383.1:p.Ile535=
XM_005271326.4:c.1605T>C	XP_005271383.1:p.Ile535=
XM_005271327.2:c.1422T>C	XP_005271384.1:p.Ile474=
XM_005271327.4:c.1422T>C	XP_005271384.1:p.Ile474=