Canonical Allele Identifier: CA365221342
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109444994A>C , CM000668.2:g.109444994A>C GRCh38
NC_000006.11:g.109766197A>C , CM000668.1:g.109766197A>C GRCh37
NC_000006.10:g.109872890A>C NCBI36
NG_042833.1:g.25975T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.2883T>G MANE Select ENSP00000351664.3:p.Ser961Arg
ENST00000358577.7:c.2625T>G ENSP00000351385.3:p.Ser875Arg
ENST00000358807.7:c.2883T>G ENSP00000351664.3:p.Ser961Arg
ENST00000456101.6:n.3662T>G
ENST00000465904.1:n.3934T>G
ENST00000630715.2:c.2940T>G ENSP00000486901.1:p.Ser980Arg
NM_001159291.1:c.2625T>G NP_001152763.1:p.Ser875Arg
NM_001286613.1:c.2940T>G NP_001273542.1:p.Ser980Arg
NM_022765.3:c.2883T>G NP_073602.3:p.Ser961Arg
NM_022765.4:c.2883T>G MANE Select NP_073602.3:p.Ser961Arg
NM_001159291.2:c.2625T>G NP_001152763.1:p.Ser875Arg
NM_001286613.2:c.2940T>G NP_001273542.1:p.Ser980Arg