Canonical Allele Identifier: CA2539443056

Gene: MICU3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.17072027A>G , CM000670.2:g.17072027A>G	GRCh38
NC_000008.10:g.16929536A>G , CM000670.1:g.16929536A>G	GRCh37
NC_000008.9:g.16973907A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000318063.10:c.567+2308A>G MANE Select	ENSP00000321455.5:n.567+2308A>G
ENST00000318063.9:c.567+2308A>G	ENSP00000321455.5:n.567+2308A>G
ENST00000517398.1:c.85+2308A>G
ENST00000517447.1:n.56+2308A>G
ENST00000519044.5:c.140+2308A>G
ENST00000522235.5:n.238-5756A>G
NM_181723.2:c.567+2308A>G	NP_859074.1:n.567+2308A>G
XM_005273477.1:c.567+2308A>G	XP_005273534.1:n.567+2308A>G
XM_006716328.1:c.567+2308A>G	XP_006716391.1:n.567+2308A>G
XM_006716329.1:c.567+2308A>G	XP_006716392.1:n.567+2308A>G
XM_006716330.1:c.567+2308A>G	XP_006716393.1:n.567+2308A>G
XM_006716331.2:c.567+2308A>G	XP_006716394.1:n.567+2308A>G
XM_006716332.2:c.567+2308A>G	XP_006716395.1:n.567+2308A>G
XM_006716333.2:c.567+2308A>G	XP_006716396.1:n.567+2308A>G
XM_006716334.2:c.567+2308A>G	XP_006716397.1:n.567+2308A>G
XM_011544507.1:c.567+2308A>G	XP_011542809.1:n.567+2308A>G
XM_011544508.1:c.567+2308A>G	XP_011542810.1:n.567+2308A>G
XR_428307.2:n.603+2308A>G
XR_428308.2:n.603+2308A>G
XR_428309.1:n.603+2308A>G
XR_949390.1:n.603+2308A>G
XR_949391.1:n.603+2308A>G
XR_949392.1:n.603+2308A>G
XR_949393.1:n.603+2308A>G
NM_001349810.1:c.567+2308A>G	NP_001336739.1:n.567+2308A>G
NR_146233.1:n.609+2308A>G
XM_005273477.2:c.567+2308A>G	XP_005273534.1:n.567+2308A>G
XM_006716328.2:c.567+2308A>G	XP_006716391.1:n.567+2308A>G
XM_006716329.2:c.567+2308A>G	XP_006716392.1:n.567+2308A>G
XM_006716330.2:c.567+2308A>G	XP_006716393.1:n.567+2308A>G
XM_006716333.3:c.567+2308A>G	XP_006716396.1:n.567+2308A>G
XM_011544508.2:c.567+2308A>G	XP_011542810.1:n.567+2308A>G
XM_017013336.1:c.567+2308A>G	XP_016868825.1:n.567+2308A>G
XM_017013337.1:c.567+2308A>G	XP_016868826.1:n.567+2308A>G
XM_017013338.1:c.567+2308A>G	XP_016868827.1:n.567+2308A>G
XM_017013339.1:c.567+2308A>G	XP_016868828.1:n.567+2308A>G
XM_017013340.1:c.40-5756A>G	XP_016868829.1:n.40-5756A>G
XM_017013341.1:c.567+2308A>G	XP_016868830.1:n.567+2308A>G
XM_017013342.1:c.40-5756A>G	XP_016868831.1:n.40-5756A>G
XM_017013343.1:c.567+2308A>G	XP_016868832.1:n.567+2308A>G
XM_024447133.1:c.567+2308A>G	XP_024302901.1:n.567+2308A>G
XM_024447134.1:c.567+2308A>G	XP_024302902.1:n.567+2308A>G
XM_024447135.1:c.567+2308A>G	XP_024302903.1:n.567+2308A>G
XR_001745513.1:n.607+2308A>G
XR_001745514.1:n.607+2308A>G
XR_001745515.2:n.607+2308A>G
XR_001745516.1:n.607+2308A>G
XR_001745517.1:n.607+2308A>G
XR_001745518.1:n.607+2308A>G
XR_001745519.1:n.607+2308A>G
XR_001745520.1:n.607+2308A>G
XR_001745521.1:n.607+2308A>G
XR_001745522.1:n.607+2308A>G
XR_949390.2:n.607+2308A>G
NM_181723.3:c.567+2308A>G MANE Select	NP_859074.1:n.567+2308A>G
NM_001349810.2:c.567+2308A>G	NP_001336739.1:n.567+2308A>G
NR_146233.2:n.609+2308A>G