Canonical Allele Identifier: CA3952632

Gene: MICAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109444235G>A , CM000668.2:g.109444235G>A	GRCh38
NC_000006.11:g.109765438G>A , CM000668.1:g.109765438G>A	GRCh37
NC_000006.10:g.109872131G>A	NCBI36
NG_042833.1:g.26734C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358807.8:c.3160C>T MANE Select	ENSP00000351664.3:p.Arg1054Cys
ENST00000358577.7:c.2902C>T	ENSP00000351385.3:p.Arg968Cys
ENST00000358807.7:c.3160C>T	ENSP00000351664.3:p.Arg1054Cys
ENST00000456101.6:n.3939C>T
ENST00000465904.1:n.4211C>T
ENST00000630715.2:c.3217C>T	ENSP00000486901.1:p.Arg1073Cys
NM_001159291.1:c.2902C>T	NP_001152763.1:p.Arg968Cys
NM_001286613.1:c.3217C>T	NP_001273542.1:p.Arg1073Cys
NM_022765.3:c.3160C>T	NP_073602.3:p.Arg1054Cys
NM_022765.4:c.3160C>T MANE Select	NP_073602.3:p.Arg1054Cys
NM_001159291.2:c.2902C>T	NP_001152763.1:p.Arg968Cys
NM_001286613.2:c.3217C>T	NP_001273542.1:p.Arg1073Cys