Canonical Allele Identifier: CA517466562

Gene: NEXMIF

Linked Data

• MyVariant Identifiers: chrX:g.73960747G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74740912G>A , CM000685.2:g.74740912G>A	GRCh38
NC_000023.10:g.73960747G>A , CM000685.1:g.73960747G>A	GRCh37
NC_000023.9:g.73877472G>A	NCBI36
NG_027726.1:g.189541C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000055682.12:c.3645C>T MANE Select	ENSP00000055682.5:p.Asn1215=
ENST00000616200.2:c.3645C>T	ENSP00000480284.1:p.Asn1215=
ENST00000642681.2:c.3645C>T	ENSP00000495800.1:p.Asn1215=
ENST00000055682.10:c.3645C>T	ENSP00000055682.5:p.Asn1215=
ENST00000616200.1:c.3645C>T	ENSP00000480284.1:p.Asn1215=
NM_001008537.2:c.3645C>T	NP_001008537.1:p.Asn1215=
XM_011530935.1:c.3645C>T	XP_011529237.1:p.Asn1215=
NM_001008537.3:c.3645C>T MANE Select	NP_001008537.1:p.Asn1215=