Canonical Allele Identifier: CA2573055403
Gene: NEXMIF HGNC NCBI

Linked Data

ClinVar Variation Id: 1335779
ClinVar RCV Id: RCV001816545
dbSNP Id: rs2147439257

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740851dup , CM000685.2:g.74740851dup GRCh38
NC_000023.10:g.73960686dup , CM000685.1:g.73960686dup GRCh37
NC_000023.9:g.73877411dup NCBI36
NG_027726.1:g.189605dup

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3709dup MANE Select ENSP00000055682.5:p.Met1237AsnfsTer24
ENST00000616200.2:c.3709dup ENSP00000480284.1:p.Met1237AsnfsTer24
ENST00000642681.2:c.3709dup ENSP00000495800.1:p.Met1237AsnfsTer24
ENST00000055682.10:c.3709dup ENSP00000055682.5:p.Met1237AsnfsTer24
ENST00000616200.1:c.3709dup ENSP00000480284.1:p.Met1237AsnfsTer24
NM_001008537.2:c.3709dup NP_001008537.1:p.Met1237AsnfsTer24
XM_011530935.1:c.3709dup XP_011529237.1:p.Met1237AsnfsTer24
NM_001008537.3:c.3709dup MANE Select NP_001008537.1:p.Met1237AsnfsTer24