Canonical Allele Identifier: CA350043478
Gene: NDUFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206127903G>A , CM000664.2:g.206127903G>A GRCh38
NC_000002.11:g.206992627G>A , CM000664.1:g.206992627G>A GRCh37
NC_000002.10:g.206700872G>A NCBI36
NG_009248.1:g.36561C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.1778C>T MANE Select ENSP00000233190.5:p.Ser593Phe
ENST00000233190.10:c.1778C>T ENSP00000233190.5:p.Ser593Phe
ENST00000423725.5:c.1607C>T ENSP00000397760.1:p.Ser536Phe
ENST00000432169.5:c.1445C>T ENSP00000409689.1:p.Ser482Phe
ENST00000440274.5:c.1670C>T ENSP00000409766.1:p.Ser557Phe
ENST00000449699.5:c.1778C>T ENSP00000399912.1:p.Ser593Phe
ENST00000455934.6:c.1820C>T ENSP00000392709.2:p.Ser607Phe
ENST00000457011.5:c.1430C>T ENSP00000400976.1:p.Ser477Phe
ENST00000498520.1:n.250C>T
NM_001199981.1:c.1670C>T NP_001186910.1:p.Ser557Phe
NM_001199982.1:c.1445C>T NP_001186911.1:p.Ser482Phe
NM_001199983.1:c.1607C>T NP_001186912.1:p.Ser536Phe
NM_001199984.1:c.1820C>T NP_001186913.1:p.Ser607Phe
NM_005006.6:c.1778C>T NP_004997.4:p.Ser593Phe
XM_017004188.2:c.1019C>T XP_016859677.1:p.Ser340Phe
NM_001199981.2:c.1670C>T NP_001186910.1:p.Ser557Phe
NM_001199982.2:c.1445C>T NP_001186911.1:p.Ser482Phe
NM_001199983.2:c.1607C>T NP_001186912.1:p.Ser536Phe
NM_005006.7:c.1778C>T MANE Select NP_004997.4:p.Ser593Phe
NM_001199984.2:c.1820C>T NP_001186913.1:p.Ser607Phe