Canonical Allele Identifier: CA2395344424
Gene: MICAL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17957142G= , CM000684.2:g.17957142G= GRCh38
NC_000022.10:g.18439908G= , CM000684.1:g.18439908G= GRCh37
NC_000022.9:g.16819908G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000441493.7:c.-74-50256C= MANE Select ENSP00000416015.2:n.-74-50256C=
ENST00000672019.1:c.-74-50256C= ENSP00000500702.1:n.-74-50256C=
ENST00000424046.1:c.-75+43947C= ENSP00000406193.1:n.-75+43947C=
ENST00000441493.6:c.-74-50256C= ENSP00000416015.2:n.-74-50256C=
ENST00000495076.5:c.-75+44251C= ENSP00000434678.1:n.-75+44251C=
NM_015241.2:c.-74-50256C= NP_056056.2:n.-74-50256C=
XM_005261262.2:c.-75+44251C= XP_005261319.1:n.-75+44251C=
XM_006724081.2:c.-75+44251C= XP_006724144.1:n.-75+44251C=
XM_006724086.2:c.-75+44251C= XP_006724149.1:n.-75+44251C=
XM_011546135.1:c.-74-50256C= XP_011544437.1:n.-74-50256C=
XM_011546137.1:c.-75+44251C= XP_011544439.1:n.-75+44251C=
XM_011546138.1:c.-75+44251C= XP_011544440.1:n.-75+44251C=
XM_011546139.1:c.-75+44251C= XP_011544441.1:n.-75+44251C=
XM_011546140.1:c.-75+44251C= XP_011544442.1:n.-75+44251C=
XM_011546141.1:c.-75+44251C= XP_011544443.1:n.-75+44251C=
XM_011546142.1:c.-75+44251C= XP_011544444.1:n.-75+44251C=
XM_011546143.1:c.-75+44251C= XP_011544445.1:n.-75+44251C=
XM_011546144.1:c.-75+44251C= XP_011544446.1:n.-75+44251C=
XM_011546145.1:c.-75+44251C= XP_011544447.1:n.-75+44251C=
XM_011546146.1:c.-75+44251C= XP_011544448.1:n.-75+44251C=
XM_011546147.1:c.-75+44251C= XP_011544449.1:n.-75+44251C=
XM_011546148.1:c.-75+44251C= XP_011544450.1:n.-75+44251C=
XR_951208.1:n.89+44251C=
XR_951209.1:n.89+44251C=
XM_005261262.3:c.-75+44251C= XP_005261319.1:n.-75+44251C=
XM_011546137.2:c.-75+44251C= XP_011544439.1:n.-75+44251C=
XM_011546139.3:c.-75+44251C= XP_011544441.1:n.-75+44251C=
XM_011546142.2:c.-75+44251C= XP_011544444.1:n.-75+44251C=
XM_011546146.3:c.-75+44251C= XP_011544448.1:n.-75+44251C=
XM_017028865.2:c.-75+28184C= XP_016884354.1:n.-75+28184C=
XM_017028868.2:c.-74-50256C= XP_016884357.1:n.-74-50256C=
XM_017028872.2:c.-75+44251C= XP_016884361.1:n.-75+44251C=
XM_017028873.2:c.-75+44251C= XP_016884362.1:n.-75+44251C=
XM_017028874.2:c.-75+44251C= XP_016884363.1:n.-75+44251C=
XM_017028875.2:c.-75+44251C= XP_016884364.1:n.-75+44251C=
XM_017028876.2:c.-75+44251C= XP_016884365.1:n.-75+44251C=
XM_017028877.2:c.-75+44251C= XP_016884366.1:n.-75+44251C=
XM_017028878.2:c.-75+44251C= XP_016884367.1:n.-75+44251C=
XM_017028879.2:c.-75+44251C= XP_016884368.1:n.-75+44251C=
XM_017028881.2:c.-74-50256C= XP_016884370.1:n.-74-50256C=
XM_017028882.2:c.-75+44251C= XP_016884371.1:n.-75+44251C=
XM_017028887.2:c.-75+44251C= XP_016884376.1:n.-75+44251C=
XR_001755266.1:n.109+44251C=
XR_951208.2:n.109+44251C=
XR_951209.2:n.109+44251C=
NM_015241.3:c.-74-50256C= MANE Select NP_056056.2:n.-74-50256C=