Canonical Allele Identifier: CA2753996702

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206123262_206123263insA , CM000664.2:g.206123262_206123263insA	GRCh38
NC_000002.11:g.206987986_206987987insA , CM000664.1:g.206987986_206987987insA	GRCh37
NC_000002.10:g.206696231_206696232insA	NCBI36
NG_009248.1:g.41201_41202insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.*922_*923insT MANE Select	ENSP00000233190.5:n.*922_*923insT
ENST00000233190.10:c.*922_*923insT	ENSP00000233190.5:n.*922_*923insT
ENST00000455934.6:c.*922_*923insT	ENSP00000392709.2:n.*922_*923insT
NM_001199981.1:c.*922_*923insT	NP_001186910.1:n.*922_*923insT
NM_001199982.1:c.*922_*923insT	NP_001186911.1:n.*922_*923insT
NM_001199983.1:c.*922_*923insT	NP_001186912.1:n.*922_*923insT
NM_001199984.1:c.*922_*923insT	NP_001186913.1:n.*922_*923insT
NM_005006.6:c.*922_*923insT	NP_004997.4:n.*922_*923insT
NM_001199981.2:c.*922_*923insT	NP_001186910.1:n.*922_*923insT
NM_001199982.2:c.*922_*923insT	NP_001186911.1:n.*922_*923insT
NM_001199983.2:c.*922_*923insT	NP_001186912.1:n.*922_*923insT
NM_005006.7:c.*922_*923insT MANE Select	NP_004997.4:n.*922_*923insT
NM_001199984.2:c.*922_*923insT	NP_001186913.1:n.*922_*923insT