Canonical Allele Identifier: CA2662803112

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206123263-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206123263C>T , CM000664.2:g.206123263C>T	GRCh38
NC_000002.11:g.206987987C>T , CM000664.1:g.206987987C>T	GRCh37
NC_000002.10:g.206696232C>T	NCBI36
NG_009248.1:g.41201G>A

Transcript Alleles

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