Canonical Allele Identifier: CA68048797
Community Standard Title: NM_004544.4(NDUFA10):c.*428C>T
Gene: NDUFA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.239960690G>A , CM000664.2:g.239960690G>A GRCh38
NC_000002.11:g.240900107G>A , CM000664.1:g.240900107G>A GRCh37
NC_000002.10:g.240548780G>A NCBI36
NG_031855.1:g.69713C>T
NG_031855.2:g.69713C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004544.4:c.*428C>T MANE Select NP_004535.1:n.*428C>T
ENST00000252711.7:c.*428C>T MANE Select ENSP00000252711.2:n.*428C>T
NM_001322020.1:c.*433C>T NP_001308949.1:n.*433C>T
NM_001322020.2:c.*433C>T NP_001308949.1:n.*433C>T
NM_004544.3:c.*428C>T NP_004535.1:n.*428C>T
NR_136155.1:n.4639C>T
NR_136155.2:n.4579C>T
NR_136156.1:n.4530C>T
NR_136156.2:n.4470C>T
NR_136157.1:n.4470C>T
NR_136157.2:n.4410C>T
NR_136158.1:n.4033+44520C>T
NR_136158.2:n.3973+44520C>T
ENST00000252711.6:c.*428C>T ENSP00000252711.2:n.*428C>T
ENST00000419408.5:c.294+29384C>T ENSP00000408055.1:n.294+29384C>T
ENST00000471378.1:n.82-1653C>T
ENST00000476216.6:n.4635C>T
ENST00000676491.1:c.1000-1653C>T ENSP00000504528.1:n.1000-1653C>T
ENST00000676782.1:c.1000-21980C>T ENSP00000504717.1:n.1000-21980C>T
ENST00000676929.1:c.*95+333C>T ENSP00000503956.1:n.*95+333C>T
ENST00000677057.1:n.4028+44520C>T
ENST00000677155.1:c.*685C>T ENSP00000502921.1:n.*685C>T
ENST00000677294.1:c.*428C>T ENSP00000503461.1:n.*428C>T
ENST00000677324.1:n.3993C>T
ENST00000677395.1:c.*3192C>T ENSP00000502890.1:n.*3192C>T
ENST00000677407.1:c.1000-9672C>T ENSP00000503141.1:n.1000-9672C>T
ENST00000677692.1:n.4260+265C>T
ENST00000677764.1:c.*807C>T ENSP00000504547.1:n.*807C>T
ENST00000677979.1:c.*975C>T ENSP00000503341.1:n.*975C>T
ENST00000678158.1:c.*163+265C>T ENSP00000504765.1:n.*163+265C>T
ENST00000678188.1:n.4717C>T
ENST00000678455.1:c.*428C>T ENSP00000504395.1:n.*428C>T
ENST00000678468.1:c.*1034C>T ENSP00000503925.1:n.*1034C>T
ENST00000678562.1:c.*4331C>T ENSP00000502954.1:n.*4331C>T
ENST00000678832.1:c.*1152C>T ENSP00000502992.1:n.*1152C>T
ENST00000678914.1:c.*428C>T ENSP00000504515.1:n.*428C>T
ENST00000679183.1:c.999+29384C>T ENSP00000503016.1:n.999+29384C>T
XM_011511229.1:c.*433C>T XP_011509531.1:n.*433C>T