Canonical Allele Identifier: CA3952631
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109444241_109444243del , CM000668.2:g.109444241_109444243del GRCh38
NC_000006.11:g.109765444_109765446del , CM000668.1:g.109765444_109765446del GRCh37
NC_000006.10:g.109872137_109872139del NCBI36
NG_042833.1:g.26731_26733del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.3157_3159del MANE Select ENSP00000351664.3:p.Glu1053del
ENST00000358577.7:c.2899_2901del ENSP00000351385.3:p.Glu967del
ENST00000358807.7:c.3157_3159del ENSP00000351664.3:p.Glu1053del
ENST00000456101.6:n.3936_3938del
ENST00000465904.1:n.4208_4210del
ENST00000630715.2:c.3214_3216del ENSP00000486901.1:p.Glu1072del
NM_001159291.1:c.2899_2901del NP_001152763.1:p.Glu967del
NM_001286613.1:c.3214_3216del NP_001273542.1:p.Glu1072del
NM_022765.3:c.3157_3159del NP_073602.3:p.Glu1053del
NM_022765.4:c.3157_3159del MANE Select NP_073602.3:p.Glu1053del
NM_001159291.2:c.2899_2901del NP_001152763.1:p.Glu967del
NM_001286613.2:c.3214_3216del NP_001273542.1:p.Glu1072del