Canonical Allele Identifier: CA365221282
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109444968C>T , CM000668.2:g.109444968C>T GRCh38
NC_000006.11:g.109766171C>T , CM000668.1:g.109766171C>T GRCh37
NC_000006.10:g.109872864C>T NCBI36
NG_042833.1:g.26001G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.2909G>A MANE Select ENSP00000351664.3:p.Trp970Ter
ENST00000358577.7:c.2651G>A ENSP00000351385.3:p.Trp884Ter
ENST00000358807.7:c.2909G>A ENSP00000351664.3:p.Trp970Ter
ENST00000456101.6:n.3688G>A
ENST00000465904.1:n.3960G>A
ENST00000630715.2:c.2966G>A ENSP00000486901.1:p.Trp989Ter
NM_001159291.1:c.2651G>A NP_001152763.1:p.Trp884Ter
NM_001286613.1:c.2966G>A NP_001273542.1:p.Trp989Ter
NM_022765.3:c.2909G>A NP_073602.3:p.Trp970Ter
NM_022765.4:c.2909G>A MANE Select NP_073602.3:p.Trp970Ter
NM_001159291.2:c.2651G>A NP_001152763.1:p.Trp884Ter
NM_001286613.2:c.2966G>A NP_001273542.1:p.Trp989Ter