Canonical Allele Identifier: CA1041598563
Gene: NDUFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1692110006

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206145107_206145108insAAAA , CM000664.2:g.206145107_206145108insAAAA GRCh38
NC_000002.11:g.207009831_207009832insAAAA , CM000664.1:g.207009831_207009832insAAAA GRCh37
NC_000002.10:g.206718076_206718077insAAAA NCBI36
NG_009248.1:g.19356_19357insTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.738-82_738-81insTTTT MANE Select ENSP00000233190.5:n.738-82_738-81insTTTT
ENST00000233190.10:c.738-82_738-81insTTTT ENSP00000233190.5:n.738-82_738-81insTTTT
ENST00000423725.5:c.567-82_567-81insTTTT ENSP00000397760.1:n.567-82_567-81insTTTT
ENST00000432169.5:c.405-82_405-81insTTTT ENSP00000409689.1:n.405-82_405-81insTTTT
ENST00000440274.5:c.630-82_630-81insTTTT ENSP00000409766.1:n.630-82_630-81insTTTT
ENST00000449699.5:c.738-82_738-81insTTTT ENSP00000399912.1:n.738-82_738-81insTTTT
ENST00000455934.6:c.780-82_780-81insTTTT ENSP00000392709.2:n.780-82_780-81insTTTT
ENST00000457011.5:c.390-82_390-81insTTTT ENSP00000400976.1:n.390-82_390-81insTTTT
NM_001199981.1:c.630-82_630-81insTTTT NP_001186910.1:n.630-82_630-81insTTTT
NM_001199982.1:c.405-82_405-81insTTTT NP_001186911.1:n.405-82_405-81insTTTT
NM_001199983.1:c.567-82_567-81insTTTT NP_001186912.1:n.567-82_567-81insTTTT
NM_001199984.1:c.780-82_780-81insTTTT NP_001186913.1:n.780-82_780-81insTTTT
NM_005006.6:c.738-82_738-81insTTTT NP_004997.4:n.738-82_738-81insTTTT
XM_017004188.2:c.-53-51_-53-50insTTTT XP_016859677.1:n.-53-51_-53-50insTTTT
NM_001199981.2:c.630-82_630-81insTTTT NP_001186910.1:n.630-82_630-81insTTTT
NM_001199982.2:c.405-82_405-81insTTTT NP_001186911.1:n.405-82_405-81insTTTT
NM_001199983.2:c.567-82_567-81insTTTT NP_001186912.1:n.567-82_567-81insTTTT
NM_005006.7:c.738-82_738-81insTTTT MANE Select NP_004997.4:n.738-82_738-81insTTTT
NM_001199984.2:c.780-82_780-81insTTTT NP_001186913.1:n.780-82_780-81insTTTT