Canonical Allele Identifier: CA68048533
Community Standard Title: NM_004544.4(NDUFA10):c.*679A>G
Gene: NDUFA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.239960439T>C , CM000664.2:g.239960439T>C GRCh38
NC_000002.11:g.240899856T>C , CM000664.1:g.240899856T>C GRCh37
NC_000002.10:g.240548529T>C NCBI36
NG_031855.1:g.69964A>G
NG_031855.2:g.69964A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004544.4:c.*679A>G MANE Select NP_004535.1:n.*679A>G
ENST00000252711.7:c.*679A>G MANE Select ENSP00000252711.2:n.*679A>G
NM_001322020.1:c.*684A>G NP_001308949.1:n.*684A>G
NM_001322020.2:c.*684A>G NP_001308949.1:n.*684A>G
NM_004544.3:c.*679A>G NP_004535.1:n.*679A>G
NR_136155.1:n.4890A>G
NR_136155.2:n.4830A>G
NR_136156.1:n.4781A>G
NR_136156.2:n.4721A>G
NR_136157.1:n.4721A>G
NR_136157.2:n.4661A>G
NR_136158.1:n.4033+44771A>G
NR_136158.2:n.3973+44771A>G
ENST00000252711.6:c.*679A>G ENSP00000252711.2:n.*679A>G
ENST00000419408.5:c.294+29635A>G ENSP00000408055.1:n.294+29635A>G
ENST00000471378.1:n.82-1402A>G
ENST00000476216.6:n.4886A>G
ENST00000676491.1:c.1000-1402A>G ENSP00000504528.1:n.1000-1402A>G
ENST00000676782.1:c.1000-21729A>G ENSP00000504717.1:n.1000-21729A>G
ENST00000676929.1:c.*95+584A>G ENSP00000503956.1:n.*95+584A>G
ENST00000677057.1:n.4028+44771A>G
ENST00000677155.1:c.*936A>G ENSP00000502921.1:n.*936A>G
ENST00000677294.1:c.*679A>G ENSP00000503461.1:n.*679A>G
ENST00000677324.1:n.4244A>G
ENST00000677395.1:c.*3443A>G ENSP00000502890.1:n.*3443A>G
ENST00000677407.1:c.1000-9421A>G ENSP00000503141.1:n.1000-9421A>G
ENST00000677692.1:n.4260+516A>G
ENST00000677764.1:c.*1058A>G ENSP00000504547.1:n.*1058A>G
ENST00000677979.1:c.*1226A>G ENSP00000503341.1:n.*1226A>G
ENST00000678158.1:c.*163+516A>G ENSP00000504765.1:n.*163+516A>G
ENST00000678188.1:n.4968A>G
ENST00000678455.1:c.*679A>G ENSP00000504395.1:n.*679A>G
ENST00000678468.1:c.*1285A>G ENSP00000503925.1:n.*1285A>G
ENST00000678562.1:c.*4582A>G ENSP00000502954.1:n.*4582A>G
ENST00000678832.1:c.*1403A>G ENSP00000502992.1:n.*1403A>G
ENST00000678914.1:c.*679A>G ENSP00000504515.1:n.*679A>G
ENST00000679183.1:c.999+29635A>G ENSP00000503016.1:n.999+29635A>G
XM_011511229.1:c.*684A>G XP_011509531.1:n.*684A>G