Canonical Allele Identifier: CA209546783

Gene: MICU1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72375969T>C , CM000672.2:g.72375969T>C	GRCh38
NC_000010.10:g.74135727T>C , CM000672.1:g.74135727T>C	GRCh37
NC_000010.9:g.73805733T>C	NCBI36
NG_033179.1:g.255223A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001195518.2:c.1181-97A>G MANE Select	NP_001182447.1:n.1181-97A>G
ENST00000361114.10:c.1181-97A>G MANE Select	ENSP00000354415.5:n.1181-97A>G
NM_001195518.1:c.1181-97A>G	NP_001182447.1:n.1181-97A>G
NM_001195519.1:c.587-97A>G	NP_001182448.1:n.587-97A>G
NM_001195519.2:c.587-97A>G	NP_001182448.1:n.587-97A>G
NM_001363513.1:c.1199-97A>G	NP_001350442.1:n.1199-97A>G
NM_001363513.2:c.1199-97A>G	NP_001350442.1:n.1199-97A>G
NM_006077.3:c.1187-97A>G	NP_006068.2:n.1187-97A>G
NM_006077.4:c.1187-97A>G	NP_006068.2:n.1187-97A>G
ENST00000361114.9:c.1181-97A>G	ENSP00000354415.5:n.1181-97A>G
ENST00000398761.8:c.1187-97A>G	ENSP00000381745.5:n.1187-97A>G
ENST00000398763.8:c.587-97A>G	ENSP00000381747.4:n.587-97A>G
ENST00000418483.6:c.587-97A>G	ENSP00000402470.2:n.587-97A>G
ENST00000476605.7:c.828-97A>G
ENST00000635239.1:c.1193-97A>G	ENSP00000489563.1:n.1193-97A>G
ENST00000642044.1:c.1199-97A>G	ENSP00000493232.1:n.1199-97A>G
XM_005269383.1:c.1199-97A>G	XP_005269440.1:n.1199-97A>G
XM_005269384.1:c.1193-97A>G	XP_005269441.1:n.1193-97A>G
XM_005269386.1:c.497-97A>G	XP_005269443.1:n.497-97A>G
XM_005269386.2:c.497-97A>G	XP_005269443.1:n.497-97A>G
XM_011539119.1:c.1349-97A>G	XP_011537421.1:n.1349-97A>G
XR_001746993.2:n.1557-97A>G
XR_001746994.2:n.1395-97A>G
XR_945585.1:n.1556-97A>G
XR_945586.1:n.1388-97A>G
XR_945586.2:n.1389-97A>G