Canonical Allele Identifier: CA365221138
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109444902A>G , CM000668.2:g.109444902A>G GRCh38
NC_000006.11:g.109766105A>G , CM000668.1:g.109766105A>G GRCh37
NC_000006.10:g.109872798A>G NCBI36
NG_042833.1:g.26067T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.2975T>C MANE Select ENSP00000351664.3:p.Met992Thr
ENST00000358577.7:c.2717T>C ENSP00000351385.3:p.Met906Thr
ENST00000358807.7:c.2975T>C ENSP00000351664.3:p.Met992Thr
ENST00000456101.6:n.3754T>C
ENST00000465904.1:n.4026T>C
ENST00000630715.2:c.3032T>C ENSP00000486901.1:p.Met1011Thr
NM_001159291.1:c.2717T>C NP_001152763.1:p.Met906Thr
NM_001286613.1:c.3032T>C NP_001273542.1:p.Met1011Thr
NM_022765.3:c.2975T>C NP_073602.3:p.Met992Thr
NM_022765.4:c.2975T>C MANE Select NP_073602.3:p.Met992Thr
NM_001159291.2:c.2717T>C NP_001152763.1:p.Met906Thr
NM_001286613.2:c.3032T>C NP_001273542.1:p.Met1011Thr