Canonical Allele Identifier: CA517466154

Gene: NEXMIF

Linked Data

• MyVariant Identifiers: chrX:g.73960843C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74741008C>T , CM000685.2:g.74741008C>T	GRCh38
NC_000023.10:g.73960843C>T , CM000685.1:g.73960843C>T	GRCh37
NC_000023.9:g.73877568C>T	NCBI36
NG_027726.1:g.189445G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000055682.12:c.3549G>A MANE Select	ENSP00000055682.5:p.Lys1183=
ENST00000616200.2:c.3549G>A	ENSP00000480284.1:p.Lys1183=
ENST00000642681.2:c.3549G>A	ENSP00000495800.1:p.Lys1183=
ENST00000055682.10:c.3549G>A	ENSP00000055682.5:p.Lys1183=
ENST00000616200.1:c.3549G>A	ENSP00000480284.1:p.Lys1183=
NM_001008537.2:c.3549G>A	NP_001008537.1:p.Lys1183=
XM_011530935.1:c.3549G>A	XP_011529237.1:p.Lys1183=
NM_001008537.3:c.3549G>A MANE Select	NP_001008537.1:p.Lys1183=