Canonical Allele Identifier: CA2753997230

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145124_206145125insA , CM000664.2:g.206145124_206145125insA	GRCh38
NC_000002.11:g.207009848_207009849insA , CM000664.1:g.207009848_207009849insA	GRCh37
NC_000002.10:g.206718093_206718094insA	NCBI36
NG_009248.1:g.19339_19340insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.738-99_738-98insT MANE Select	ENSP00000233190.5:n.738-99_738-98insT
ENST00000233190.10:c.738-99_738-98insT	ENSP00000233190.5:n.738-99_738-98insT
ENST00000423725.5:c.567-99_567-98insT	ENSP00000397760.1:n.567-99_567-98insT
ENST00000432169.5:c.405-99_405-98insT	ENSP00000409689.1:n.405-99_405-98insT
ENST00000440274.5:c.630-99_630-98insT	ENSP00000409766.1:n.630-99_630-98insT
ENST00000449699.5:c.738-99_738-98insT	ENSP00000399912.1:n.738-99_738-98insT
ENST00000455934.6:c.780-99_780-98insT	ENSP00000392709.2:n.780-99_780-98insT
ENST00000457011.5:c.390-99_390-98insT	ENSP00000400976.1:n.390-99_390-98insT
NM_001199981.1:c.630-99_630-98insT	NP_001186910.1:n.630-99_630-98insT
NM_001199982.1:c.405-99_405-98insT	NP_001186911.1:n.405-99_405-98insT
NM_001199983.1:c.567-99_567-98insT	NP_001186912.1:n.567-99_567-98insT
NM_001199984.1:c.780-99_780-98insT	NP_001186913.1:n.780-99_780-98insT
NM_005006.6:c.738-99_738-98insT	NP_004997.4:n.738-99_738-98insT
XM_017004188.2:c.-53-68_-53-67insT	XP_016859677.1:n.-53-68_-53-67insT
NM_001199981.2:c.630-99_630-98insT	NP_001186910.1:n.630-99_630-98insT
NM_001199982.2:c.405-99_405-98insT	NP_001186911.1:n.405-99_405-98insT
NM_001199983.2:c.567-99_567-98insT	NP_001186912.1:n.567-99_567-98insT
NM_005006.7:c.738-99_738-98insT MANE Select	NP_004997.4:n.738-99_738-98insT
NM_001199984.2:c.780-99_780-98insT	NP_001186913.1:n.780-99_780-98insT