Canonical Allele Identifier: CA10091288

Gene: MICAL3

Linked Data

• ClinVar Variation Id: 493330
• ClinVar RCV Id: RCV000584994
• dbSNP Id: rs750739956
• ExAC: 22:18299464 G / A
• gnomAD v2: 22-18299464-G-A
• gnomAD v3: 22-17816698-G-A
• gnomAD v4: 22-17816698-G-A
• MyVariant Identifiers: chr22:g.18299464G>A (hg19) ; chr22:g.17816698G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17816698G>A , CM000684.2:g.17816698G>A	GRCh38
NC_000022.10:g.18299464G>A , CM000684.1:g.18299464G>A	GRCh37
NC_000022.9:g.16679464G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441493.7:c.5437C>T MANE Select	ENSP00000416015.2:p.Arg1813Trp
ENST00000672019.1:c.*2384C>T	ENSP00000500702.1:n.*2384C>T
ENST00000441493.6:c.5437C>T	ENSP00000416015.2:p.Arg1813Trp
ENST00000577821.5:c.266C>T
ENST00000579997.5:c.202C>T	ENSP00000462107.1:p.Arg68Trp
NM_015241.2:c.5437C>T	NP_056056.2:p.Arg1813Trp
XM_005261262.2:c.5437C>T	XP_005261319.1:p.Arg1813Trp
XM_006724081.2:c.5956C>T	XP_006724144.1:p.Arg1986Trp
XM_006724086.2:c.5818C>T	XP_006724149.1:p.Arg1940Trp
XM_011546134.1:c.5956C>T	XP_011544436.1:p.Arg1986Trp
XM_011546135.1:c.5956C>T	XP_011544437.1:p.Arg1986Trp
XM_011546136.1:c.5956C>T	XP_011544438.1:p.Arg1986Trp
XM_011546137.1:c.5956C>T	XP_011544439.1:p.Arg1986Trp
XM_011546138.1:c.5956C>T	XP_011544440.1:p.Arg1986Trp
XM_011546139.1:c.5956C>T	XP_011544441.1:p.Arg1986Trp
XM_011546140.1:c.5872C>T	XP_011544442.1:p.Arg1958Trp
XM_011546141.1:c.5848C>T	XP_011544443.1:p.Arg1950Trp
XM_011546142.1:c.5956C>T	XP_011544444.1:p.Arg1986Trp
XM_011546143.1:c.5755C>T	XP_011544445.1:p.Arg1919Trp
XM_011546144.1:c.5641C>T	XP_011544446.1:p.Arg1881Trp
XM_011546145.1:c.5500C>T	XP_011544447.1:p.Arg1834Trp
XR_951208.1:n.6119C>T
XR_951209.1:n.6119C>T
XM_005261262.3:c.5437C>T	XP_005261319.1:p.Arg1813Trp
XM_011546137.2:c.5956C>T	XP_011544439.1:p.Arg1986Trp
XM_011546139.3:c.5956C>T	XP_011544441.1:p.Arg1986Trp
XM_011546142.2:c.5956C>T	XP_011544444.1:p.Arg1986Trp
XM_017028865.2:c.5956C>T	XP_016884354.1:p.Arg1986Trp
XM_017028866.2:c.5956C>T	XP_016884355.1:p.Arg1986Trp
XM_017028867.2:c.5956C>T	XP_016884356.1:p.Arg1986Trp
XM_017028868.2:c.5956C>T	XP_016884357.1:p.Arg1986Trp
XM_017028869.2:c.5956C>T	XP_016884358.1:p.Arg1986Trp
XM_017028870.2:c.5956C>T	XP_016884359.1:p.Arg1986Trp
XM_017028872.2:c.5956C>T	XP_016884361.1:p.Arg1986Trp
XM_017028873.2:c.5893C>T	XP_016884362.1:p.Arg1965Trp
XM_017028874.2:c.5872C>T	XP_016884363.1:p.Arg1958Trp
XM_017028875.2:c.5848C>T	XP_016884364.1:p.Arg1950Trp
XM_017028876.2:c.5818C>T	XP_016884365.1:p.Arg1940Trp
XM_017028877.2:c.5755C>T	XP_016884366.1:p.Arg1919Trp
XM_017028878.2:c.5641C>T	XP_016884367.1:p.Arg1881Trp
XM_017028879.2:c.5500C>T	XP_016884368.1:p.Arg1834Trp
XM_017028880.2:c.5500C>T	XP_016884369.1:p.Arg1834Trp
XM_017028881.2:c.5500C>T	XP_016884370.1:p.Arg1834Trp
XM_017028882.2:c.5437C>T	XP_016884371.1:p.Arg1813Trp
XM_017028883.2:c.5056C>T	XP_016884372.1:p.Arg1686Trp
XM_017028884.2:c.4600C>T	XP_016884373.1:p.Arg1534Trp
XM_017028885.2:c.3253C>T	XP_016884374.1:p.Arg1085Trp
XM_017028886.2:c.3253C>T	XP_016884375.1:p.Arg1085Trp
XR_951208.2:n.6139C>T
XR_951209.2:n.6139C>T
NM_015241.3:c.5437C>T MANE Select	NP_056056.2:p.Arg1813Trp