Canonical Allele Identifier: CA413665482
Gene: NEXMIF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74741009T>G , CM000685.2:g.74741009T>G GRCh38
NC_000023.10:g.73960844T>G , CM000685.1:g.73960844T>G GRCh37
NC_000023.9:g.73877569T>G NCBI36
NG_027726.1:g.189444A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3548A>C MANE Select ENSP00000055682.5:p.Lys1183Thr
ENST00000616200.2:c.3548A>C ENSP00000480284.1:p.Lys1183Thr
ENST00000642681.2:c.3548A>C ENSP00000495800.1:p.Lys1183Thr
ENST00000055682.10:c.3548A>C ENSP00000055682.5:p.Lys1183Thr
ENST00000616200.1:c.3548A>C ENSP00000480284.1:p.Lys1183Thr
NM_001008537.2:c.3548A>C NP_001008537.1:p.Lys1183Thr
XM_011530935.1:c.3548A>C XP_011529237.1:p.Lys1183Thr
NM_001008537.3:c.3548A>C MANE Select NP_001008537.1:p.Lys1183Thr