Canonical Allele Identifier: CA2496476590
Gene: NDUFS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206122534C= , CM000664.2:g.206122534C= GRCh38
NC_000002.11:g.206987258C= , CM000664.1:g.206987258C= GRCh37
NC_000002.10:g.206695503C= NCBI36
NG_009248.1:g.41930G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.*1651G= MANE Select ENSP00000233190.5:n.*1651G=
ENST00000233190.10:c.*1651G= ENSP00000233190.5:n.*1651G=
NM_001199981.2:c.*1651G= NP_001186910.1:n.*1651G=
NM_001199982.2:c.*1651G= NP_001186911.1:n.*1651G=
NM_001199983.2:c.*1651G= NP_001186912.1:n.*1651G=
NM_005006.7:c.*1651G= MANE Select NP_004997.4:n.*1651G=
NM_001199984.2:c.*1651G= NP_001186913.1:n.*1651G=
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