Canonical Allele Identifier: CA5550015

Gene: MICU1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72375757T>A , CM000672.2:g.72375757T>A	GRCh38
NC_000010.10:g.74135515T>A , CM000672.1:g.74135515T>A	GRCh37
NC_000010.9:g.73805521T>A	NCBI36
NG_033179.1:g.255435A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361114.10:c.1270+26A>T MANE Select	ENSP00000354415.5:n.1270+26A>T
ENST00000642044.1:c.1288+26A>T	ENSP00000493232.1:n.1288+26A>T
ENST00000361114.9:c.1270+26A>T	ENSP00000354415.5:n.1270+26A>T
ENST00000398761.8:c.1276+26A>T	ENSP00000381745.5:n.1276+26A>T
ENST00000398763.8:c.676+26A>T	ENSP00000381747.4:n.676+26A>T
ENST00000418483.6:c.676+26A>T	ENSP00000402470.2:n.676+26A>T
ENST00000476605.7:c.917+26A>T
ENST00000635239.1:c.1282+26A>T	ENSP00000489563.1:n.1282+26A>T
NM_001195518.1:c.1270+26A>T	NP_001182447.1:n.1270+26A>T
NM_001195519.1:c.676+26A>T	NP_001182448.1:n.676+26A>T
NM_006077.3:c.1276+26A>T	NP_006068.2:n.1276+26A>T
XM_005269383.1:c.1288+26A>T	XP_005269440.1:n.1288+26A>T
XM_005269384.1:c.1282+26A>T	XP_005269441.1:n.1282+26A>T
XM_005269386.1:c.586+26A>T	XP_005269443.1:n.586+26A>T
XM_011539119.1:c.1438+26A>T	XP_011537421.1:n.1438+26A>T
XR_945586.1:n.1477+26A>T
NM_001363513.1:c.1288+26A>T	NP_001350442.1:n.1288+26A>T
XM_005269386.2:c.586+26A>T	XP_005269443.1:n.586+26A>T
XR_001746993.2:n.1646+26A>T
XR_001746994.2:n.1484+26A>T
XR_945586.2:n.1478+26A>T
NM_001195518.2:c.1270+26A>T MANE Select	NP_001182447.1:n.1270+26A>T
NM_001195519.2:c.676+26A>T	NP_001182448.1:n.676+26A>T
NM_001363513.2:c.1288+26A>T	NP_001350442.1:n.1288+26A>T
NM_006077.4:c.1276+26A>T	NP_006068.2:n.1276+26A>T