Canonical Allele Identifier: CA2496487371
Gene: NDUFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206144933C= , CM000664.2:g.206144933C= GRCh38
NC_000002.11:g.207009657C= , CM000664.1:g.207009657C= GRCh37
NC_000002.10:g.206717902C= NCBI36
NG_009248.1:g.19531G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.831G= MANE Select ENSP00000233190.5:p.Met277=
ENST00000233190.10:c.831G= ENSP00000233190.5:p.Met277=
ENST00000423725.5:c.660G= ENSP00000397760.1:p.Met220=
ENST00000432169.5:c.498G= ENSP00000409689.1:p.Met166=
ENST00000440274.5:c.723G= ENSP00000409766.1:p.Met241=
ENST00000449699.5:c.831G= ENSP00000399912.1:p.Met277=
ENST00000455934.6:c.873G= ENSP00000392709.2:p.Met291=
ENST00000457011.5:c.483G= ENSP00000400976.1:p.Met161=
NM_001199981.1:c.723G= NP_001186910.1:p.Met241=
NM_001199982.1:c.498G= NP_001186911.1:p.Met166=
NM_001199983.1:c.660G= NP_001186912.1:p.Met220=
NM_001199984.1:c.873G= NP_001186913.1:p.Met291=
NM_005006.6:c.831G= NP_004997.4:p.Met277=
XM_017004188.2:c.72G= XP_016859677.1:p.Met24=
NM_001199981.2:c.723G= NP_001186910.1:p.Met241=
NM_001199982.2:c.498G= NP_001186911.1:p.Met166=
NM_001199983.2:c.660G= NP_001186912.1:p.Met220=
NM_005006.7:c.831G= MANE Select NP_004997.4:p.Met277=
NM_001199984.2:c.873G= NP_001186913.1:p.Met291=