Canonical Allele Identifier: CA3952739
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109445268T>A , CM000668.2:g.109445268T>A GRCh38
NC_000006.11:g.109766471T>A , CM000668.1:g.109766471T>A GRCh37
NC_000006.10:g.109873164T>A NCBI36
NG_042833.1:g.25701A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.2810A>T MANE Select ENSP00000351664.3:p.Glu937Val
ENST00000358577.7:c.2552A>T ENSP00000351385.3:p.Glu851Val
ENST00000358807.7:c.2810A>T ENSP00000351664.3:p.Glu937Val
ENST00000456101.6:n.3589A>T
ENST00000465904.1:n.3861A>T
ENST00000630715.2:c.2867A>T ENSP00000486901.1:p.Glu956Val
NM_001159291.1:c.2552A>T NP_001152763.1:p.Glu851Val
NM_001286613.1:c.2867A>T NP_001273542.1:p.Glu956Val
NM_022765.3:c.2810A>T NP_073602.3:p.Glu937Val
NM_022765.4:c.2810A>T MANE Select NP_073602.3:p.Glu937Val
NM_001159291.2:c.2552A>T NP_001152763.1:p.Glu851Val
NM_001286613.2:c.2867A>T NP_001273542.1:p.Glu956Val