Canonical Allele Identifier: CA3952725
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109445197T>G , CM000668.2:g.109445197T>G GRCh38
NC_000006.11:g.109766400T>G , CM000668.1:g.109766400T>G GRCh37
NC_000006.10:g.109873093T>G NCBI36
NG_042833.1:g.25772A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.2881A>C MANE Select ENSP00000351664.3:p.Ser961Arg
ENST00000358577.7:c.2623A>C ENSP00000351385.3:p.Ser875Arg
ENST00000358807.7:c.2881A>C ENSP00000351664.3:p.Ser961Arg
ENST00000456101.6:n.3660A>C
ENST00000465904.1:n.3932A>C
ENST00000630715.2:c.2938A>C ENSP00000486901.1:p.Ser980Arg
NM_001159291.1:c.2623A>C NP_001152763.1:p.Ser875Arg
NM_001286613.1:c.2938A>C NP_001273542.1:p.Ser980Arg
NM_022765.3:c.2881A>C NP_073602.3:p.Ser961Arg
NM_022765.4:c.2881A>C MANE Select NP_073602.3:p.Ser961Arg
NM_001159291.2:c.2623A>C NP_001152763.1:p.Ser875Arg
NM_001286613.2:c.2938A>C NP_001273542.1:p.Ser980Arg