Canonical Allele Identifier: CA2662801079
Gene: NDUFS1 HGNC NCBI

Linked Data

dbSNP Id: rs2105945561

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206127981_206127982insTAAT , CM000664.2:g.206127981_206127982insTAAT GRCh38
NC_000002.11:g.206992705_206992706insTAAT , CM000664.1:g.206992705_206992706insTAAT GRCh37
NC_000002.10:g.206700950_206700951insTAAT NCBI36
NG_009248.1:g.36482_36483insATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.1709-10_1709-9insATTA MANE Select ENSP00000233190.5:n.1709-10_1709-9insATTA
ENST00000233190.10:c.1709-10_1709-9insATTA ENSP00000233190.5:n.1709-10_1709-9insATTA
ENST00000423725.5:c.1538-10_1538-9insATTA ENSP00000397760.1:n.1538-10_1538-9insATTA
ENST00000432169.5:c.1376-10_1376-9insATTA ENSP00000409689.1:n.1376-10_1376-9insATTA
ENST00000440274.5:c.1601-10_1601-9insATTA ENSP00000409766.1:n.1601-10_1601-9insATTA
ENST00000449699.5:c.1709-10_1709-9insATTA ENSP00000399912.1:n.1709-10_1709-9insATTA
ENST00000455934.6:c.1751-10_1751-9insATTA ENSP00000392709.2:n.1751-10_1751-9insATTA
ENST00000457011.5:c.1361-10_1361-9insATTA ENSP00000400976.1:n.1361-10_1361-9insATTA
ENST00000498520.1:n.181-10_181-9insATTA
NM_001199981.1:c.1601-10_1601-9insATTA NP_001186910.1:n.1601-10_1601-9insATTA
NM_001199982.1:c.1376-10_1376-9insATTA NP_001186911.1:n.1376-10_1376-9insATTA
NM_001199983.1:c.1538-10_1538-9insATTA NP_001186912.1:n.1538-10_1538-9insATTA
NM_001199984.1:c.1751-10_1751-9insATTA NP_001186913.1:n.1751-10_1751-9insATTA
NM_005006.6:c.1709-10_1709-9insATTA NP_004997.4:n.1709-10_1709-9insATTA
XM_017004188.2:c.950-10_950-9insATTA XP_016859677.1:n.950-10_950-9insATTA
NM_001199981.2:c.1601-10_1601-9insATTA NP_001186910.1:n.1601-10_1601-9insATTA
NM_001199982.2:c.1376-10_1376-9insATTA NP_001186911.1:n.1376-10_1376-9insATTA
NM_001199983.2:c.1538-10_1538-9insATTA NP_001186912.1:n.1538-10_1538-9insATTA
NM_005006.7:c.1709-10_1709-9insATTA MANE Select NP_004997.4:n.1709-10_1709-9insATTA
NM_001199984.2:c.1751-10_1751-9insATTA NP_001186913.1:n.1751-10_1751-9insATTA