Canonical Allele Identifier: CA517466150
Gene: NEXMIF HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73960840A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74741005A>G , CM000685.2:g.74741005A>G GRCh38
NC_000023.10:g.73960840A>G , CM000685.1:g.73960840A>G GRCh37
NC_000023.9:g.73877565A>G NCBI36
NG_027726.1:g.189448T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3552T>C MANE Select ENSP00000055682.5:p.Ser1184=
ENST00000616200.2:c.3552T>C ENSP00000480284.1:p.Ser1184=
ENST00000642681.2:c.3552T>C ENSP00000495800.1:p.Ser1184=
ENST00000055682.10:c.3552T>C ENSP00000055682.5:p.Ser1184=
ENST00000616200.1:c.3552T>C ENSP00000480284.1:p.Ser1184=
NM_001008537.2:c.3552T>C NP_001008537.1:p.Ser1184=
XM_011530935.1:c.3552T>C XP_011529237.1:p.Ser1184=
NM_001008537.3:c.3552T>C MANE Select NP_001008537.1:p.Ser1184=
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