Canonical Allele Identifier: CA350057190
Gene: NDUFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206144934A>T , CM000664.2:g.206144934A>T GRCh38
NC_000002.11:g.207009658A>T , CM000664.1:g.207009658A>T GRCh37
NC_000002.10:g.206717903A>T NCBI36
NG_009248.1:g.19530T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.830T>A MANE Select ENSP00000233190.5:p.Met277Lys
ENST00000233190.10:c.830T>A ENSP00000233190.5:p.Met277Lys
ENST00000423725.5:c.659T>A ENSP00000397760.1:p.Met220Lys
ENST00000432169.5:c.497T>A ENSP00000409689.1:p.Met166Lys
ENST00000440274.5:c.722T>A ENSP00000409766.1:p.Met241Lys
ENST00000449699.5:c.830T>A ENSP00000399912.1:p.Met277Lys
ENST00000455934.6:c.872T>A ENSP00000392709.2:p.Met291Lys
ENST00000457011.5:c.482T>A ENSP00000400976.1:p.Met161Lys
NM_001199981.1:c.722T>A NP_001186910.1:p.Met241Lys
NM_001199982.1:c.497T>A NP_001186911.1:p.Met166Lys
NM_001199983.1:c.659T>A NP_001186912.1:p.Met220Lys
NM_001199984.1:c.872T>A NP_001186913.1:p.Met291Lys
NM_005006.6:c.830T>A NP_004997.4:p.Met277Lys
XM_017004188.2:c.71T>A XP_016859677.1:p.Met24Lys
NM_001199981.2:c.722T>A NP_001186910.1:p.Met241Lys
NM_001199982.2:c.497T>A NP_001186911.1:p.Met166Lys
NM_001199983.2:c.659T>A NP_001186912.1:p.Met220Lys
NM_005006.7:c.830T>A MANE Select NP_004997.4:p.Met277Lys
NM_001199984.2:c.872T>A NP_001186913.1:p.Met291Lys