Canonical Allele Identifier: CA413664921
Gene: NEXMIF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740848T>C , CM000685.2:g.74740848T>C GRCh38
NC_000023.10:g.73960683T>C , CM000685.1:g.73960683T>C GRCh37
NC_000023.9:g.73877408T>C NCBI36
NG_027726.1:g.189605A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3709A>G MANE Select ENSP00000055682.5:p.Met1237Val
ENST00000616200.2:c.3709A>G ENSP00000480284.1:p.Met1237Val
ENST00000642681.2:c.3709A>G ENSP00000495800.1:p.Met1237Val
ENST00000055682.10:c.3709A>G ENSP00000055682.5:p.Met1237Val
ENST00000616200.1:c.3709A>G ENSP00000480284.1:p.Met1237Val
NM_001008537.2:c.3709A>G NP_001008537.1:p.Met1237Val
XM_011530935.1:c.3709A>G XP_011529237.1:p.Met1237Val
NM_001008537.3:c.3709A>G MANE Select NP_001008537.1:p.Met1237Val