Canonical Allele Identifier: CA10092749

Gene: MICAL3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17893880C>T , CM000684.2:g.17893880C>T	GRCh38
NC_000022.10:g.18376646C>T , CM000684.1:g.18376646C>T	GRCh37
NC_000022.9:g.16756646C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441493.7:c.1474G>A MANE Select	ENSP00000416015.2:p.Glu492Lys
ENST00000672019.1:c.1474G>A	ENSP00000500702.1:p.Glu492Lys
ENST00000383094.7:c.1474G>A	ENSP00000372574.3:p.Glu492Lys
ENST00000400561.6:c.1474G>A	ENSP00000383406.2:p.Glu492Lys
ENST00000414725.6:c.1474G>A	ENSP00000391827.2:p.Glu492Lys
ENST00000441493.6:c.1474G>A	ENSP00000416015.2:p.Glu492Lys
ENST00000461307.5:c.30G>A
ENST00000495076.5:c.*365G>A	ENSP00000434678.1:n.*365G>A
ENST00000585038.1:c.1474G>A	ENSP00000462033.1:p.Glu492Lys
NM_001122731.2:c.1474G>A	NP_001116203.1:p.Glu492Lys
NM_001136004.3:c.1474G>A	NP_001129476.1:p.Glu492Lys
NM_015241.2:c.1474G>A	NP_056056.2:p.Glu492Lys
XM_005261262.2:c.1474G>A	XP_005261319.1:p.Glu492Lys
XM_006724081.2:c.1474G>A	XP_006724144.1:p.Glu492Lys
XM_006724086.2:c.1474G>A	XP_006724149.1:p.Glu492Lys
XM_011546134.1:c.1474G>A	XP_011544436.1:p.Glu492Lys
XM_011546135.1:c.1474G>A	XP_011544437.1:p.Glu492Lys
XM_011546136.1:c.1474G>A	XP_011544438.1:p.Glu492Lys
XM_011546137.1:c.1474G>A	XP_011544439.1:p.Glu492Lys
XM_011546138.1:c.1474G>A	XP_011544440.1:p.Glu492Lys
XM_011546139.1:c.1474G>A	XP_011544441.1:p.Glu492Lys
XM_011546140.1:c.1474G>A	XP_011544442.1:p.Glu492Lys
XM_011546141.1:c.1474G>A	XP_011544443.1:p.Glu492Lys
XM_011546142.1:c.1474G>A	XP_011544444.1:p.Glu492Lys
XM_011546143.1:c.1474G>A	XP_011544445.1:p.Glu492Lys
XM_011546144.1:c.1474G>A	XP_011544446.1:p.Glu492Lys
XM_011546145.1:c.1474G>A	XP_011544447.1:p.Glu492Lys
XM_011546146.1:c.1474G>A	XP_011544448.1:p.Glu492Lys
XM_011546147.1:c.1474G>A	XP_011544449.1:p.Glu492Lys
XR_951208.1:n.1637G>A
XR_951209.1:n.1637G>A
XM_005261262.3:c.1474G>A	XP_005261319.1:p.Glu492Lys
XM_011546137.2:c.1474G>A	XP_011544439.1:p.Glu492Lys
XM_011546139.3:c.1474G>A	XP_011544441.1:p.Glu492Lys
XM_011546142.2:c.1474G>A	XP_011544444.1:p.Glu492Lys
XM_011546146.3:c.1474G>A	XP_011544448.1:p.Glu492Lys
XM_017028865.2:c.1474G>A	XP_016884354.1:p.Glu492Lys
XM_017028866.2:c.1474G>A	XP_016884355.1:p.Glu492Lys
XM_017028867.2:c.1474G>A	XP_016884356.1:p.Glu492Lys
XM_017028868.2:c.1474G>A	XP_016884357.1:p.Glu492Lys
XM_017028869.2:c.1474G>A	XP_016884358.1:p.Glu492Lys
XM_017028870.2:c.1474G>A	XP_016884359.1:p.Glu492Lys
XM_017028872.2:c.1474G>A	XP_016884361.1:p.Glu492Lys
XM_017028873.2:c.1474G>A	XP_016884362.1:p.Glu492Lys
XM_017028874.2:c.1474G>A	XP_016884363.1:p.Glu492Lys
XM_017028875.2:c.1474G>A	XP_016884364.1:p.Glu492Lys
XM_017028876.2:c.1474G>A	XP_016884365.1:p.Glu492Lys
XM_017028877.2:c.1474G>A	XP_016884366.1:p.Glu492Lys
XM_017028878.2:c.1474G>A	XP_016884367.1:p.Glu492Lys
XM_017028879.2:c.1474G>A	XP_016884368.1:p.Glu492Lys
XM_017028880.2:c.1474G>A	XP_016884369.1:p.Glu492Lys
XM_017028881.2:c.1474G>A	XP_016884370.1:p.Glu492Lys
XM_017028882.2:c.1474G>A	XP_016884371.1:p.Glu492Lys
XM_017028883.2:c.574G>A	XP_016884372.1:p.Glu192Lys
XM_017028884.2:c.574G>A	XP_016884373.1:p.Glu192Lys
XM_017028887.2:c.1474G>A	XP_016884376.1:p.Glu492Lys
XR_951208.2:n.1657G>A
XR_951209.2:n.1657G>A
NM_015241.3:c.1474G>A MANE Select	NP_056056.2:p.Glu492Lys