Canonical Allele Identifier: CA2753997216

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145108_206145109insAG , CM000664.2:g.206145108_206145109insAG	GRCh38
NC_000002.11:g.207009832_207009833insAG , CM000664.1:g.207009832_207009833insAG	GRCh37
NC_000002.10:g.206718077_206718078insAG	NCBI36
NG_009248.1:g.19355_19356insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.738-83_738-82insCT MANE Select	ENSP00000233190.5:n.738-83_738-82insCT
ENST00000233190.10:c.738-83_738-82insCT	ENSP00000233190.5:n.738-83_738-82insCT
ENST00000423725.5:c.567-83_567-82insCT	ENSP00000397760.1:n.567-83_567-82insCT
ENST00000432169.5:c.405-83_405-82insCT	ENSP00000409689.1:n.405-83_405-82insCT
ENST00000440274.5:c.630-83_630-82insCT	ENSP00000409766.1:n.630-83_630-82insCT
ENST00000449699.5:c.738-83_738-82insCT	ENSP00000399912.1:n.738-83_738-82insCT
ENST00000455934.6:c.780-83_780-82insCT	ENSP00000392709.2:n.780-83_780-82insCT
ENST00000457011.5:c.390-83_390-82insCT	ENSP00000400976.1:n.390-83_390-82insCT
NM_001199981.1:c.630-83_630-82insCT	NP_001186910.1:n.630-83_630-82insCT
NM_001199982.1:c.405-83_405-82insCT	NP_001186911.1:n.405-83_405-82insCT
NM_001199983.1:c.567-83_567-82insCT	NP_001186912.1:n.567-83_567-82insCT
NM_001199984.1:c.780-83_780-82insCT	NP_001186913.1:n.780-83_780-82insCT
NM_005006.6:c.738-83_738-82insCT	NP_004997.4:n.738-83_738-82insCT
XM_017004188.2:c.-53-52_-53-51insCT	XP_016859677.1:n.-53-52_-53-51insCT
NM_001199981.2:c.630-83_630-82insCT	NP_001186910.1:n.630-83_630-82insCT
NM_001199982.2:c.405-83_405-82insCT	NP_001186911.1:n.405-83_405-82insCT
NM_001199983.2:c.567-83_567-82insCT	NP_001186912.1:n.567-83_567-82insCT
NM_005006.7:c.738-83_738-82insCT MANE Select	NP_004997.4:n.738-83_738-82insCT
NM_001199984.2:c.780-83_780-82insCT	NP_001186913.1:n.780-83_780-82insCT