Canonical Allele Identifier: CA3952741
Community Standard Title: NM_022765.4(MICAL1):c.2800C>T (p.Arg934Ter)
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109445278G>A , CM000668.2:g.109445278G>A GRCh38
NC_000006.11:g.109766481G>A , CM000668.1:g.109766481G>A GRCh37
NC_000006.10:g.109873174G>A NCBI36
NG_042833.1:g.25691C>T

Transcript Alleles

HGVS Amino-acid Change
NM_022765.4:c.2800C>T MANE Select NP_073602.3:p.Arg934Ter
ENST00000358807.8:c.2800C>T MANE Select ENSP00000351664.3:p.Arg934Ter
NM_001159291.1:c.2542C>T NP_001152763.1:p.Arg848Ter
NM_001159291.2:c.2542C>T NP_001152763.1:p.Arg848Ter
NM_001286613.1:c.2857C>T NP_001273542.1:p.Arg953Ter
NM_001286613.2:c.2857C>T NP_001273542.1:p.Arg953Ter
NM_022765.3:c.2800C>T NP_073602.3:p.Arg934Ter
ENST00000358577.7:c.2542C>T ENSP00000351385.3:p.Arg848Ter
ENST00000358807.7:c.2800C>T ENSP00000351664.3:p.Arg934Ter
ENST00000456101.6:n.3579C>T
ENST00000465904.1:n.3851C>T
ENST00000630715.2:c.2857C>T ENSP00000486901.1:p.Arg953Ter