Canonical Allele Identifier: CA2753997255

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145137_206145138insAG , CM000664.2:g.206145137_206145138insAG	GRCh38
NC_000002.11:g.207009861_207009862insAG , CM000664.1:g.207009861_207009862insAG	GRCh37
NC_000002.10:g.206718106_206718107insAG	NCBI36
NG_009248.1:g.19326_19327insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.738-112_738-111insCT MANE Select	ENSP00000233190.5:n.738-112_738-111insCT
ENST00000233190.10:c.738-112_738-111insCT	ENSP00000233190.5:n.738-112_738-111insCT
ENST00000423725.5:c.567-112_567-111insCT	ENSP00000397760.1:n.567-112_567-111insCT
ENST00000432169.5:c.405-112_405-111insCT	ENSP00000409689.1:n.405-112_405-111insCT
ENST00000440274.5:c.630-112_630-111insCT	ENSP00000409766.1:n.630-112_630-111insCT
ENST00000449699.5:c.738-112_738-111insCT	ENSP00000399912.1:n.738-112_738-111insCT
ENST00000455934.6:c.780-112_780-111insCT	ENSP00000392709.2:n.780-112_780-111insCT
ENST00000457011.5:c.390-112_390-111insCT	ENSP00000400976.1:n.390-112_390-111insCT
NM_001199981.1:c.630-112_630-111insCT	NP_001186910.1:n.630-112_630-111insCT
NM_001199982.1:c.405-112_405-111insCT	NP_001186911.1:n.405-112_405-111insCT
NM_001199983.1:c.567-112_567-111insCT	NP_001186912.1:n.567-112_567-111insCT
NM_001199984.1:c.780-112_780-111insCT	NP_001186913.1:n.780-112_780-111insCT
NM_005006.6:c.738-112_738-111insCT	NP_004997.4:n.738-112_738-111insCT
XM_017004188.2:c.-53-81_-53-80insCT	XP_016859677.1:n.-53-81_-53-80insCT
NM_001199981.2:c.630-112_630-111insCT	NP_001186910.1:n.630-112_630-111insCT
NM_001199982.2:c.405-112_405-111insCT	NP_001186911.1:n.405-112_405-111insCT
NM_001199983.2:c.567-112_567-111insCT	NP_001186912.1:n.567-112_567-111insCT
NM_005006.7:c.738-112_738-111insCT MANE Select	NP_004997.4:n.738-112_738-111insCT
NM_001199984.2:c.780-112_780-111insCT	NP_001186913.1:n.780-112_780-111insCT