Canonical Allele Identifier: CA350057334
Gene: NDUFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206144953T>A , CM000664.2:g.206144953T>A GRCh38
NC_000002.11:g.207009677T>A , CM000664.1:g.207009677T>A GRCh37
NC_000002.10:g.206717922T>A NCBI36
NG_009248.1:g.19511A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.811A>T MANE Select ENSP00000233190.5:p.Met271Leu
ENST00000233190.10:c.811A>T ENSP00000233190.5:p.Met271Leu
ENST00000423725.5:c.640A>T ENSP00000397760.1:p.Met214Leu
ENST00000432169.5:c.478A>T ENSP00000409689.1:p.Met160Leu
ENST00000440274.5:c.703A>T ENSP00000409766.1:p.Met235Leu
ENST00000449699.5:c.811A>T ENSP00000399912.1:p.Met271Leu
ENST00000455934.6:c.853A>T ENSP00000392709.2:p.Met285Leu
ENST00000457011.5:c.463A>T ENSP00000400976.1:p.Met155Leu
NM_001199981.1:c.703A>T NP_001186910.1:p.Met235Leu
NM_001199982.1:c.478A>T NP_001186911.1:p.Met160Leu
NM_001199983.1:c.640A>T NP_001186912.1:p.Met214Leu
NM_001199984.1:c.853A>T NP_001186913.1:p.Met285Leu
NM_005006.6:c.811A>T NP_004997.4:p.Met271Leu
XM_017004188.2:c.52A>T XP_016859677.1:p.Met18Leu
NM_001199981.2:c.703A>T NP_001186910.1:p.Met235Leu
NM_001199982.2:c.478A>T NP_001186911.1:p.Met160Leu
NM_001199983.2:c.640A>T NP_001186912.1:p.Met214Leu
NM_005006.7:c.811A>T MANE Select NP_004997.4:p.Met271Leu
NM_001199984.2:c.853A>T NP_001186913.1:p.Met285Leu