Canonical Allele Identifier: CA1041598576
Gene: NDUFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1692110675

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206145144dup , CM000664.2:g.206145144dup GRCh38
NC_000002.11:g.207009868dup , CM000664.1:g.207009868dup GRCh37
NC_000002.10:g.206718113dup NCBI36
NG_009248.1:g.19325dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.738-113dup MANE Select ENSP00000233190.5:n.738-113dup
ENST00000233190.10:c.738-113dup ENSP00000233190.5:n.738-113dup
ENST00000423725.5:c.567-113dup ENSP00000397760.1:n.567-113dup
ENST00000432169.5:c.405-113dup ENSP00000409689.1:n.405-113dup
ENST00000440274.5:c.630-113dup ENSP00000409766.1:n.630-113dup
ENST00000449699.5:c.738-113dup ENSP00000399912.1:n.738-113dup
ENST00000455934.6:c.780-113dup ENSP00000392709.2:n.780-113dup
ENST00000457011.5:c.390-113dup ENSP00000400976.1:n.390-113dup
NM_001199981.1:c.630-113dup NP_001186910.1:n.630-113dup
NM_001199982.1:c.405-113dup NP_001186911.1:n.405-113dup
NM_001199983.1:c.567-113dup NP_001186912.1:n.567-113dup
NM_001199984.1:c.780-113dup NP_001186913.1:n.780-113dup
NM_005006.6:c.738-113dup NP_004997.4:n.738-113dup
XM_017004188.2:c.-53-82dup XP_016859677.1:n.-53-82dup
NM_001199981.2:c.630-113dup NP_001186910.1:n.630-113dup
NM_001199982.2:c.405-113dup NP_001186911.1:n.405-113dup
NM_001199983.2:c.567-113dup NP_001186912.1:n.567-113dup
NM_005006.7:c.738-113dup MANE Select NP_004997.4:n.738-113dup
NM_001199984.2:c.780-113dup NP_001186913.1:n.780-113dup