Canonical Allele Identifier: CA2753997251

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145135_206145136insAGA , CM000664.2:g.206145135_206145136insAGA	GRCh38
NC_000002.11:g.207009859_207009860insAGA , CM000664.1:g.207009859_207009860insAGA	GRCh37
NC_000002.10:g.206718104_206718105insAGA	NCBI36
NG_009248.1:g.19328_19329insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.738-110_738-109insTCT MANE Select	ENSP00000233190.5:n.738-110_738-109insTCT
ENST00000233190.10:c.738-110_738-109insTCT	ENSP00000233190.5:n.738-110_738-109insTCT
ENST00000423725.5:c.567-110_567-109insTCT	ENSP00000397760.1:n.567-110_567-109insTCT
ENST00000432169.5:c.405-110_405-109insTCT	ENSP00000409689.1:n.405-110_405-109insTCT
ENST00000440274.5:c.630-110_630-109insTCT	ENSP00000409766.1:n.630-110_630-109insTCT
ENST00000449699.5:c.738-110_738-109insTCT	ENSP00000399912.1:n.738-110_738-109insTCT
ENST00000455934.6:c.780-110_780-109insTCT	ENSP00000392709.2:n.780-110_780-109insTCT
ENST00000457011.5:c.390-110_390-109insTCT	ENSP00000400976.1:n.390-110_390-109insTCT
NM_001199981.1:c.630-110_630-109insTCT	NP_001186910.1:n.630-110_630-109insTCT
NM_001199982.1:c.405-110_405-109insTCT	NP_001186911.1:n.405-110_405-109insTCT
NM_001199983.1:c.567-110_567-109insTCT	NP_001186912.1:n.567-110_567-109insTCT
NM_001199984.1:c.780-110_780-109insTCT	NP_001186913.1:n.780-110_780-109insTCT
NM_005006.6:c.738-110_738-109insTCT	NP_004997.4:n.738-110_738-109insTCT
XM_017004188.2:c.-53-79_-53-78insTCT	XP_016859677.1:n.-53-79_-53-78insTCT
NM_001199981.2:c.630-110_630-109insTCT	NP_001186910.1:n.630-110_630-109insTCT
NM_001199982.2:c.405-110_405-109insTCT	NP_001186911.1:n.405-110_405-109insTCT
NM_001199983.2:c.567-110_567-109insTCT	NP_001186912.1:n.567-110_567-109insTCT
NM_005006.7:c.738-110_738-109insTCT MANE Select	NP_004997.4:n.738-110_738-109insTCT
NM_001199984.2:c.780-110_780-109insTCT	NP_001186913.1:n.780-110_780-109insTCT