Canonical Allele Identifier: CA10091641

Gene: MICAL3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17818424G>A , CM000684.2:g.17818424G>A	GRCh38
NC_000022.10:g.18301190G>A , CM000684.1:g.18301190G>A	GRCh37
NC_000022.9:g.16681190G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441493.7:c.4237C>T MANE Select	ENSP00000416015.2:p.Arg1413Cys
ENST00000672019.1:c.*1184C>T	ENSP00000500702.1:n.*1184C>T
ENST00000441493.6:c.4237C>T	ENSP00000416015.2:p.Arg1413Cys
NM_015241.2:c.4237C>T	NP_056056.2:p.Arg1413Cys
XM_005261262.2:c.4237C>T	XP_005261319.1:p.Arg1413Cys
XM_006724081.2:c.4756C>T	XP_006724144.1:p.Arg1586Cys
XM_006724086.2:c.4618C>T	XP_006724149.1:p.Arg1540Cys
XM_011546134.1:c.4756C>T	XP_011544436.1:p.Arg1586Cys
XM_011546135.1:c.4756C>T	XP_011544437.1:p.Arg1586Cys
XM_011546136.1:c.4756C>T	XP_011544438.1:p.Arg1586Cys
XM_011546137.1:c.4756C>T	XP_011544439.1:p.Arg1586Cys
XM_011546138.1:c.4756C>T	XP_011544440.1:p.Arg1586Cys
XM_011546139.1:c.4756C>T	XP_011544441.1:p.Arg1586Cys
XM_011546140.1:c.4672C>T	XP_011544442.1:p.Arg1558Cys
XM_011546141.1:c.4648C>T	XP_011544443.1:p.Arg1550Cys
XM_011546142.1:c.4756C>T	XP_011544444.1:p.Arg1586Cys
XM_011546143.1:c.4555C>T	XP_011544445.1:p.Arg1519Cys
XM_011546144.1:c.4441C>T	XP_011544446.1:p.Arg1481Cys
XM_011546145.1:c.4300C>T	XP_011544447.1:p.Arg1434Cys
XR_951208.1:n.4919C>T
XR_951209.1:n.4919C>T
XM_005261262.3:c.4237C>T	XP_005261319.1:p.Arg1413Cys
XM_011546137.2:c.4756C>T	XP_011544439.1:p.Arg1586Cys
XM_011546139.3:c.4756C>T	XP_011544441.1:p.Arg1586Cys
XM_011546142.2:c.4756C>T	XP_011544444.1:p.Arg1586Cys
XM_017028865.2:c.4756C>T	XP_016884354.1:p.Arg1586Cys
XM_017028866.2:c.4756C>T	XP_016884355.1:p.Arg1586Cys
XM_017028867.2:c.4756C>T	XP_016884356.1:p.Arg1586Cys
XM_017028868.2:c.4756C>T	XP_016884357.1:p.Arg1586Cys
XM_017028869.2:c.4756C>T	XP_016884358.1:p.Arg1586Cys
XM_017028870.2:c.4756C>T	XP_016884359.1:p.Arg1586Cys
XM_017028872.2:c.4756C>T	XP_016884361.1:p.Arg1586Cys
XM_017028873.2:c.4693C>T	XP_016884362.1:p.Arg1565Cys
XM_017028874.2:c.4672C>T	XP_016884363.1:p.Arg1558Cys
XM_017028875.2:c.4648C>T	XP_016884364.1:p.Arg1550Cys
XM_017028876.2:c.4618C>T	XP_016884365.1:p.Arg1540Cys
XM_017028877.2:c.4555C>T	XP_016884366.1:p.Arg1519Cys
XM_017028878.2:c.4441C>T	XP_016884367.1:p.Arg1481Cys
XM_017028879.2:c.4300C>T	XP_016884368.1:p.Arg1434Cys
XM_017028880.2:c.4300C>T	XP_016884369.1:p.Arg1434Cys
XM_017028881.2:c.4300C>T	XP_016884370.1:p.Arg1434Cys
XM_017028882.2:c.4237C>T	XP_016884371.1:p.Arg1413Cys
XM_017028883.2:c.3856C>T	XP_016884372.1:p.Arg1286Cys
XM_017028884.2:c.3400C>T	XP_016884373.1:p.Arg1134Cys
XM_017028885.2:c.2053C>T	XP_016884374.1:p.Arg685Cys
XM_017028886.2:c.2053C>T	XP_016884375.1:p.Arg685Cys
XR_951208.2:n.4939C>T
XR_951209.2:n.4939C>T
NM_015241.3:c.4237C>T MANE Select	NP_056056.2:p.Arg1413Cys