Canonical Allele Identifier: CA2753997223
Gene: NDUFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206145121_206145128del , CM000664.2:g.206145121_206145128del GRCh38
NC_000002.11:g.207009845_207009852del , CM000664.1:g.207009845_207009852del GRCh37
NC_000002.10:g.206718090_206718097del NCBI36
NG_009248.1:g.19337_19344del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.738-101_738-94del MANE Select ENSP00000233190.5:n.738-101_738-94del
ENST00000233190.10:c.738-101_738-94del ENSP00000233190.5:n.738-101_738-94del
ENST00000423725.5:c.567-101_567-94del ENSP00000397760.1:n.567-101_567-94del
ENST00000432169.5:c.405-101_405-94del ENSP00000409689.1:n.405-101_405-94del
ENST00000440274.5:c.630-101_630-94del ENSP00000409766.1:n.630-101_630-94del
ENST00000449699.5:c.738-101_738-94del ENSP00000399912.1:n.738-101_738-94del
ENST00000455934.6:c.780-101_780-94del ENSP00000392709.2:n.780-101_780-94del
ENST00000457011.5:c.390-101_390-94del ENSP00000400976.1:n.390-101_390-94del
NM_001199981.1:c.630-101_630-94del NP_001186910.1:n.630-101_630-94del
NM_001199982.1:c.405-101_405-94del NP_001186911.1:n.405-101_405-94del
NM_001199983.1:c.567-101_567-94del NP_001186912.1:n.567-101_567-94del
NM_001199984.1:c.780-101_780-94del NP_001186913.1:n.780-101_780-94del
NM_005006.6:c.738-101_738-94del NP_004997.4:n.738-101_738-94del
XM_017004188.2:c.-53-70_-53-63del XP_016859677.1:n.-53-70_-53-63del
NM_001199981.2:c.630-101_630-94del NP_001186910.1:n.630-101_630-94del
NM_001199982.2:c.405-101_405-94del NP_001186911.1:n.405-101_405-94del
NM_001199983.2:c.567-101_567-94del NP_001186912.1:n.567-101_567-94del
NM_005006.7:c.738-101_738-94del MANE Select NP_004997.4:n.738-101_738-94del
NM_001199984.2:c.780-101_780-94del NP_001186913.1:n.780-101_780-94del