Canonical Allele Identifier: CA2496489260
Gene: NDUFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206149032G= , CM000664.2:g.206149032G= GRCh38
NC_000002.11:g.207013756G= , CM000664.1:g.207013756G= GRCh37
NC_000002.10:g.206722001G= NCBI36
NG_009248.1:g.15432C=

Transcript Alleles

HGVS Amino-acid change
ENST00000233190.11:c.326C= MANE Select ENSP00000233190.5:p.Ser109=
ENST00000233190.10:c.326C= ENSP00000233190.5:p.Ser109=
ENST00000423725.5:c.155C= ENSP00000397760.1:p.Ser52=
ENST00000432169.5:c.6-1198C= ENSP00000409689.1:n.6-1198C=
ENST00000440274.5:c.218C= ENSP00000409766.1:p.Ser73=
ENST00000449699.5:c.326C= ENSP00000399912.1:p.Ser109=
ENST00000454195.1:c.326C= ENSP00000389413.1:p.Ser109=
ENST00000455934.6:c.368C= ENSP00000392709.2:p.Ser123=
ENST00000456284.5:c.*88C= ENSP00000395553.1:n.*88C=
ENST00000457011.5:c.-10-1198C= ENSP00000400976.1:n.-10-1198C=
NM_001199981.1:c.218C= NP_001186910.1:p.Ser73=
NM_001199982.1:c.6-1198C= NP_001186911.1:n.6-1198C=
NM_001199983.1:c.155C= NP_001186912.1:p.Ser52=
NM_001199984.1:c.368C= NP_001186913.1:p.Ser123=
NM_005006.6:c.326C= NP_004997.4:p.Ser109=
XM_017004188.2:c.-465C= XP_016859677.1:n.-465C=
NM_001199981.2:c.218C= NP_001186910.1:p.Ser73=
NM_001199982.2:c.6-1198C= NP_001186911.1:n.6-1198C=
NM_001199983.2:c.155C= NP_001186912.1:p.Ser52=
NM_005006.7:c.326C= MANE Select NP_004997.4:p.Ser109=
NM_001199984.2:c.368C= NP_001186913.1:p.Ser123=