Canonical Allele Identifier: CA2753997279

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145175_206145176insAGT , CM000664.2:g.206145175_206145176insAGT	GRCh38
NC_000002.11:g.207009899_207009900insAGT , CM000664.1:g.207009899_207009900insAGT	GRCh37
NC_000002.10:g.206718144_206718145insAGT	NCBI36
NG_009248.1:g.19288_19289insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.738-150_738-149insACT MANE Select	ENSP00000233190.5:n.738-150_738-149insACT
ENST00000233190.10:c.738-150_738-149insACT	ENSP00000233190.5:n.738-150_738-149insACT
ENST00000423725.5:c.567-150_567-149insACT	ENSP00000397760.1:n.567-150_567-149insACT
ENST00000432169.5:c.405-150_405-149insACT	ENSP00000409689.1:n.405-150_405-149insACT
ENST00000440274.5:c.630-150_630-149insACT	ENSP00000409766.1:n.630-150_630-149insACT
ENST00000449699.5:c.738-150_738-149insACT	ENSP00000399912.1:n.738-150_738-149insACT
ENST00000455934.6:c.780-150_780-149insACT	ENSP00000392709.2:n.780-150_780-149insACT
ENST00000457011.5:c.390-150_390-149insACT	ENSP00000400976.1:n.390-150_390-149insACT
NM_001199981.1:c.630-150_630-149insACT	NP_001186910.1:n.630-150_630-149insACT
NM_001199982.1:c.405-150_405-149insACT	NP_001186911.1:n.405-150_405-149insACT
NM_001199983.1:c.567-150_567-149insACT	NP_001186912.1:n.567-150_567-149insACT
NM_001199984.1:c.780-150_780-149insACT	NP_001186913.1:n.780-150_780-149insACT
NM_005006.6:c.738-150_738-149insACT	NP_004997.4:n.738-150_738-149insACT
XM_017004188.2:c.-53-119_-53-118insACT	XP_016859677.1:n.-53-119_-53-118insACT
NM_001199981.2:c.630-150_630-149insACT	NP_001186910.1:n.630-150_630-149insACT
NM_001199982.2:c.405-150_405-149insACT	NP_001186911.1:n.405-150_405-149insACT
NM_001199983.2:c.567-150_567-149insACT	NP_001186912.1:n.567-150_567-149insACT
NM_005006.7:c.738-150_738-149insACT MANE Select	NP_004997.4:n.738-150_738-149insACT
NM_001199984.2:c.780-150_780-149insACT	NP_001186913.1:n.780-150_780-149insACT