Canonical Allele Identifier: CA413664704
Gene: NEXMIF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740748G>T , CM000685.2:g.74740748G>T GRCh38
NC_000023.10:g.73960583G>T , CM000685.1:g.73960583G>T GRCh37
NC_000023.9:g.73877308G>T NCBI36
NG_027726.1:g.189705C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3809C>A MANE Select ENSP00000055682.5:p.Ser1270Tyr
ENST00000616200.2:c.3809C>A ENSP00000480284.1:p.Ser1270Tyr
ENST00000642681.2:c.3809C>A ENSP00000495800.1:p.Ser1270Tyr
ENST00000055682.10:c.3809C>A ENSP00000055682.5:p.Ser1270Tyr
ENST00000616200.1:c.3809C>A ENSP00000480284.1:p.Ser1270Tyr
NM_001008537.2:c.3809C>A NP_001008537.1:p.Ser1270Tyr
XM_011530935.1:c.3809C>A XP_011529237.1:p.Ser1270Tyr
NM_001008537.3:c.3809C>A MANE Select NP_001008537.1:p.Ser1270Tyr