Canonical Allele Identifier: CA517466253
Gene: NEXMIF HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73960585G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740750G>A , CM000685.2:g.74740750G>A GRCh38
NC_000023.10:g.73960585G>A , CM000685.1:g.73960585G>A GRCh37
NC_000023.9:g.73877310G>A NCBI36
NG_027726.1:g.189703C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3807C>T MANE Select ENSP00000055682.5:p.Ala1269=
ENST00000616200.2:c.3807C>T ENSP00000480284.1:p.Ala1269=
ENST00000642681.2:c.3807C>T ENSP00000495800.1:p.Ala1269=
ENST00000055682.10:c.3807C>T ENSP00000055682.5:p.Ala1269=
ENST00000616200.1:c.3807C>T ENSP00000480284.1:p.Ala1269=
NM_001008537.2:c.3807C>T NP_001008537.1:p.Ala1269=
XM_011530935.1:c.3807C>T XP_011529237.1:p.Ala1269=
NM_001008537.3:c.3807C>T MANE Select NP_001008537.1:p.Ala1269=