Canonical Allele Identifier: CA2437590167
Gene: NEXMIF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740913T= , CM000685.2:g.74740913T= GRCh38
NC_000023.10:g.73960748T= , CM000685.1:g.73960748T= GRCh37
NC_000023.9:g.73877473T= NCBI36
NG_027726.1:g.189540A=

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3644A= MANE Select ENSP00000055682.5:p.Asn1215=
ENST00000616200.2:c.3644A= ENSP00000480284.1:p.Asn1215=
ENST00000642681.2:c.3644A= ENSP00000495800.1:p.Asn1215=
ENST00000055682.10:c.3644A= ENSP00000055682.5:p.Asn1215=
ENST00000616200.1:c.3644A= ENSP00000480284.1:p.Asn1215=
NM_001008537.2:c.3644A= NP_001008537.1:p.Asn1215=
XM_011530935.1:c.3644A= XP_011529237.1:p.Asn1215=
NM_001008537.3:c.3644A= MANE Select NP_001008537.1:p.Asn1215=