Canonical Allele Identifier: CA2662804006
Gene: NDUFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206145072_206145073insCA , CM000664.2:g.206145072_206145073insCA GRCh38
NC_000002.11:g.207009796_207009797insCA , CM000664.1:g.207009796_207009797insCA GRCh37
NC_000002.10:g.206718041_206718042insCA NCBI36
NG_009248.1:g.19391_19392insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.738-47_738-46insTG MANE Select ENSP00000233190.5:n.738-47_738-46insTG
ENST00000233190.10:c.738-47_738-46insTG ENSP00000233190.5:n.738-47_738-46insTG
ENST00000423725.5:c.567-47_567-46insTG ENSP00000397760.1:n.567-47_567-46insTG
ENST00000432169.5:c.405-47_405-46insTG ENSP00000409689.1:n.405-47_405-46insTG
ENST00000440274.5:c.630-47_630-46insTG ENSP00000409766.1:n.630-47_630-46insTG
ENST00000449699.5:c.738-47_738-46insTG ENSP00000399912.1:n.738-47_738-46insTG
ENST00000455934.6:c.780-47_780-46insTG ENSP00000392709.2:n.780-47_780-46insTG
ENST00000457011.5:c.390-47_390-46insTG ENSP00000400976.1:n.390-47_390-46insTG
NM_001199981.1:c.630-47_630-46insTG NP_001186910.1:n.630-47_630-46insTG
NM_001199982.1:c.405-47_405-46insTG NP_001186911.1:n.405-47_405-46insTG
NM_001199983.1:c.567-47_567-46insTG NP_001186912.1:n.567-47_567-46insTG
NM_001199984.1:c.780-47_780-46insTG NP_001186913.1:n.780-47_780-46insTG
NM_005006.6:c.738-47_738-46insTG NP_004997.4:n.738-47_738-46insTG
XM_017004188.2:c.-53-16_-53-15insTG XP_016859677.1:n.-53-16_-53-15insTG
NM_001199981.2:c.630-47_630-46insTG NP_001186910.1:n.630-47_630-46insTG
NM_001199982.2:c.405-47_405-46insTG NP_001186911.1:n.405-47_405-46insTG
NM_001199983.2:c.567-47_567-46insTG NP_001186912.1:n.567-47_567-46insTG
NM_005006.7:c.738-47_738-46insTG MANE Select NP_004997.4:n.738-47_738-46insTG
NM_001199984.2:c.780-47_780-46insTG NP_001186913.1:n.780-47_780-46insTG