Canonical Allele Identifier: CA2662800423
Gene: NDUFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206127621_206127623del , CM000664.2:g.206127621_206127623del GRCh38
NC_000002.11:g.206992345_206992347del , CM000664.1:g.206992345_206992347del GRCh37
NC_000002.10:g.206700590_206700592del NCBI36
NG_009248.1:g.36841_36843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.1884+174_1884+176del MANE Select ENSP00000233190.5:n.1884+174_1884+176del
ENST00000233190.10:c.1884+174_1884+176del ENSP00000233190.5:n.1884+174_1884+176del
ENST00000423725.5:c.1713+174_1713+176del ENSP00000397760.1:n.1713+174_1713+176del
ENST00000432169.5:c.1551+174_1551+176del ENSP00000409689.1:n.1551+174_1551+176del
ENST00000440274.5:c.1776+174_1776+176del ENSP00000409766.1:n.1776+174_1776+176del
ENST00000449699.5:c.1884+174_1884+176del ENSP00000399912.1:n.1884+174_1884+176del
ENST00000455934.6:c.1926+174_1926+176del ENSP00000392709.2:n.1926+174_1926+176del
ENST00000457011.5:c.1536+174_1536+176del ENSP00000400976.1:n.1536+174_1536+176del
ENST00000498520.1:n.530_532del
NM_001199981.1:c.1776+174_1776+176del NP_001186910.1:n.1776+174_1776+176del
NM_001199982.1:c.1551+174_1551+176del NP_001186911.1:n.1551+174_1551+176del
NM_001199983.1:c.1713+174_1713+176del NP_001186912.1:n.1713+174_1713+176del
NM_001199984.1:c.1926+174_1926+176del NP_001186913.1:n.1926+174_1926+176del
NM_005006.6:c.1884+174_1884+176del NP_004997.4:n.1884+174_1884+176del
XM_017004188.2:c.1125+174_1125+176del XP_016859677.1:n.1125+174_1125+176del
NM_001199981.2:c.1776+174_1776+176del NP_001186910.1:n.1776+174_1776+176del
NM_001199982.2:c.1551+174_1551+176del NP_001186911.1:n.1551+174_1551+176del
NM_001199983.2:c.1713+174_1713+176del NP_001186912.1:n.1713+174_1713+176del
NM_005006.7:c.1884+174_1884+176del MANE Select NP_004997.4:n.1884+174_1884+176del
NM_001199984.2:c.1926+174_1926+176del NP_001186913.1:n.1926+174_1926+176del