Canonical Allele Identifier: CA5550369

Gene: MICU1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72566793T>C , CM000672.2:g.72566793T>C	GRCh38
NC_000010.10:g.74326551T>C , CM000672.1:g.74326551T>C	GRCh37
NC_000010.9:g.73996557T>C	NCBI36
NG_033179.1:g.64399A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361114.10:c.1A>G MANE Select	ENSP00000354415.5:p.Met1Val
ENST00000642044.1:c.1A>G	ENSP00000493232.1:p.Met1Val
ENST00000361114.9:c.1A>G	ENSP00000354415.5:p.Met1Val
ENST00000398761.8:c.1A>G	ENSP00000381745.5:p.Met1Val
ENST00000603011.5:c.-68-34A>G	ENSP00000474192.1:n.-68-34A>G
ENST00000604025.1:n.67A>G
ENST00000604238.2:c.1A>G	ENSP00000474775.2:p.Met1Val
ENST00000635239.1:c.1A>G	ENSP00000489563.1:p.Met1Val
NM_001195518.1:c.1A>G	NP_001182447.1:p.Met1Val
NM_006077.3:c.1A>G	NP_006068.2:p.Met1Val
XM_005269383.1:c.1A>G	XP_005269440.1:p.Met1Val
XM_005269384.1:c.1A>G	XP_005269441.1:p.Met1Val
XM_011539119.1:c.1A>G	XP_011537421.1:p.Met1Val
XR_945585.1:n.88A>G
XR_945586.1:n.88A>G
NM_001363513.1:c.1A>G	NP_001350442.1:p.Met1Val
XR_001746993.2:n.89A>G
XR_001746994.2:n.89A>G
XR_945586.2:n.89A>G
NM_001195518.2:c.1A>G MANE Select	NP_001182447.1:p.Met1Val
NM_001363513.2:c.1A>G	NP_001350442.1:p.Met1Val
NM_006077.4:c.1A>G	NP_006068.2:p.Met1Val