Canonical Allele Identifier: CA2753997271

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145158_206145159insGTC , CM000664.2:g.206145158_206145159insGTC	GRCh38
NC_000002.11:g.207009882_207009883insGTC , CM000664.1:g.207009882_207009883insGTC	GRCh37
NC_000002.10:g.206718127_206718128insGTC	NCBI36
NG_009248.1:g.19305_19306insGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.738-133_738-132insGAC MANE Select	ENSP00000233190.5:n.738-133_738-132insGAC
ENST00000233190.10:c.738-133_738-132insGAC	ENSP00000233190.5:n.738-133_738-132insGAC
ENST00000423725.5:c.567-133_567-132insGAC	ENSP00000397760.1:n.567-133_567-132insGAC
ENST00000432169.5:c.405-133_405-132insGAC	ENSP00000409689.1:n.405-133_405-132insGAC
ENST00000440274.5:c.630-133_630-132insGAC	ENSP00000409766.1:n.630-133_630-132insGAC
ENST00000449699.5:c.738-133_738-132insGAC	ENSP00000399912.1:n.738-133_738-132insGAC
ENST00000455934.6:c.780-133_780-132insGAC	ENSP00000392709.2:n.780-133_780-132insGAC
ENST00000457011.5:c.390-133_390-132insGAC	ENSP00000400976.1:n.390-133_390-132insGAC
NM_001199981.1:c.630-133_630-132insGAC	NP_001186910.1:n.630-133_630-132insGAC
NM_001199982.1:c.405-133_405-132insGAC	NP_001186911.1:n.405-133_405-132insGAC
NM_001199983.1:c.567-133_567-132insGAC	NP_001186912.1:n.567-133_567-132insGAC
NM_001199984.1:c.780-133_780-132insGAC	NP_001186913.1:n.780-133_780-132insGAC
NM_005006.6:c.738-133_738-132insGAC	NP_004997.4:n.738-133_738-132insGAC
XM_017004188.2:c.-53-102_-53-101insGAC	XP_016859677.1:n.-53-102_-53-101insGAC
NM_001199981.2:c.630-133_630-132insGAC	NP_001186910.1:n.630-133_630-132insGAC
NM_001199982.2:c.405-133_405-132insGAC	NP_001186911.1:n.405-133_405-132insGAC
NM_001199983.2:c.567-133_567-132insGAC	NP_001186912.1:n.567-133_567-132insGAC
NM_005006.7:c.738-133_738-132insGAC MANE Select	NP_004997.4:n.738-133_738-132insGAC
NM_001199984.2:c.780-133_780-132insGAC	NP_001186913.1:n.780-133_780-132insGAC