Canonical Allele Identifier: CA3952771
Community Standard Title: NM_022765.4(MICAL1):c.2787+12G>A
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109445404C>T , CM000668.2:g.109445404C>T GRCh38
NC_000006.11:g.109766607C>T , CM000668.1:g.109766607C>T GRCh37
NC_000006.10:g.109873300C>T NCBI36
NG_042833.1:g.25565G>A

Transcript Alleles

HGVS Amino-acid Change
NM_022765.4:c.2787+12G>A MANE Select NP_073602.3:n.2787+12G>A
ENST00000358807.8:c.2787+12G>A MANE Select ENSP00000351664.3:n.2787+12G>A
NM_001159291.1:c.2529+12G>A NP_001152763.1:n.2529+12G>A
NM_001159291.2:c.2529+12G>A NP_001152763.1:n.2529+12G>A
NM_001286613.1:c.2844+12G>A NP_001273542.1:n.2844+12G>A
NM_001286613.2:c.2844+12G>A NP_001273542.1:n.2844+12G>A
NM_022765.3:c.2787+12G>A NP_073602.3:n.2787+12G>A
ENST00000358577.7:c.2529+12G>A ENSP00000351385.3:n.2529+12G>A
ENST00000358807.7:c.2787+12G>A ENSP00000351664.3:n.2787+12G>A
ENST00000456101.6:n.3566+12G>A
ENST00000465904.1:n.3838+12G>A
ENST00000630715.2:c.2844+12G>A ENSP00000486901.1:n.2844+12G>A