Canonical Allele Identifier: CA5550109

Gene: MICU1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72423385A>T , CM000672.2:g.72423385A>T	GRCh38
NC_000010.10:g.74183143A>T , CM000672.1:g.74183143A>T	GRCh37
NC_000010.9:g.73853149A>T	NCBI36
NG_033179.1:g.207807T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001195518.2:c.934-14T>A MANE Select	NP_001182447.1:n.934-14T>A
ENST00000361114.10:c.934-14T>A MANE Select	ENSP00000354415.5:n.934-14T>A
NM_001195518.1:c.934-14T>A	NP_001182447.1:n.934-14T>A
NM_001195519.1:c.340-14T>A	NP_001182448.1:n.340-14T>A
NM_001195519.2:c.340-14T>A	NP_001182448.1:n.340-14T>A
NM_001363513.1:c.952-14T>A	NP_001350442.1:n.952-14T>A
NM_001363513.2:c.952-14T>A	NP_001350442.1:n.952-14T>A
NM_006077.3:c.940-14T>A	NP_006068.2:n.940-14T>A
NM_006077.4:c.940-14T>A	NP_006068.2:n.940-14T>A
ENST00000361114.9:c.934-14T>A	ENSP00000354415.5:n.934-14T>A
ENST00000398761.8:c.940-14T>A	ENSP00000381745.5:n.940-14T>A
ENST00000398763.8:c.340-14T>A	ENSP00000381747.4:n.340-14T>A
ENST00000418483.6:c.340-14T>A	ENSP00000402470.2:n.340-14T>A
ENST00000476605.7:c.461-14T>A
ENST00000489666.2:c.340-14T>A	ENSP00000474809.1:n.340-14T>A
ENST00000635239.1:c.946-14T>A	ENSP00000489563.1:n.946-14T>A
ENST00000642044.1:c.952-14T>A	ENSP00000493232.1:n.952-14T>A
XM_005269383.1:c.952-14T>A	XP_005269440.1:n.952-14T>A
XM_005269384.1:c.946-14T>A	XP_005269441.1:n.946-14T>A
XM_005269386.1:c.250-14T>A	XP_005269443.1:n.250-14T>A
XM_005269386.2:c.250-14T>A	XP_005269443.1:n.250-14T>A
XM_011539119.1:c.1102-14T>A	XP_011537421.1:n.1102-14T>A
XR_001746993.2:n.1190-14T>A
XR_001746994.2:n.1028-14T>A
XR_945585.1:n.1189-14T>A
XR_945586.1:n.1021-14T>A
XR_945586.2:n.1022-14T>A