Canonical Allele Identifier: CA3952732
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109445243T>C , CM000668.2:g.109445243T>C GRCh38
NC_000006.11:g.109766446T>C , CM000668.1:g.109766446T>C GRCh37
NC_000006.10:g.109873139T>C NCBI36
NG_042833.1:g.25726A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.2835A>G MANE Select ENSP00000351664.3:p.Leu945=
ENST00000358577.7:c.2577A>G ENSP00000351385.3:p.Leu859=
ENST00000358807.7:c.2835A>G ENSP00000351664.3:p.Leu945=
ENST00000456101.6:n.3614A>G
ENST00000465904.1:n.3886A>G
ENST00000630715.2:c.2892A>G ENSP00000486901.1:p.Leu964=
NM_001159291.1:c.2577A>G NP_001152763.1:p.Leu859=
NM_001286613.1:c.2892A>G NP_001273542.1:p.Leu964=
NM_022765.3:c.2835A>G NP_073602.3:p.Leu945=
NM_022765.4:c.2835A>G MANE Select NP_073602.3:p.Leu945=
NM_001159291.2:c.2577A>G NP_001152763.1:p.Leu859=
NM_001286613.2:c.2892A>G NP_001273542.1:p.Leu964=