Canonical Allele Identifier: CA3952695
Gene: MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109444910G>A , CM000668.2:g.109444910G>A GRCh38
NC_000006.11:g.109766113G>A , CM000668.1:g.109766113G>A GRCh37
NC_000006.10:g.109872806G>A NCBI36
NG_042833.1:g.26059C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358807.8:c.2967C>T MANE Select ENSP00000351664.3:p.Ala989=
ENST00000358577.7:c.2709C>T ENSP00000351385.3:p.Ala903=
ENST00000358807.7:c.2967C>T ENSP00000351664.3:p.Ala989=
ENST00000456101.6:n.3746C>T
ENST00000465904.1:n.4018C>T
ENST00000630715.2:c.3024C>T ENSP00000486901.1:p.Ala1008=
NM_001159291.1:c.2709C>T NP_001152763.1:p.Ala903=
NM_001286613.1:c.3024C>T NP_001273542.1:p.Ala1008=
NM_022765.3:c.2967C>T NP_073602.3:p.Ala989=
NM_022765.4:c.2967C>T MANE Select NP_073602.3:p.Ala989=
NM_001159291.2:c.2709C>T NP_001152763.1:p.Ala903=
NM_001286613.2:c.3024C>T NP_001273542.1:p.Ala1008=