Canonical Allele Identifier: CA2496487331

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1692095309

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144826del , CM000664.2:g.206144826del	GRCh38
NC_000002.11:g.207009550del , CM000664.1:g.207009550del	GRCh37
NC_000002.10:g.206717795del	NCBI36
NG_009248.1:g.19639del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.872+67del MANE Select	ENSP00000233190.5:n.872+67del
ENST00000233190.10:c.872+67del	ENSP00000233190.5:n.872+67del
ENST00000423725.5:c.701+67del	ENSP00000397760.1:n.701+67del
ENST00000432169.5:c.539+67del	ENSP00000409689.1:n.539+67del
ENST00000440274.5:c.764+67del	ENSP00000409766.1:n.764+67del
ENST00000449699.5:c.872+67del	ENSP00000399912.1:n.872+67del
ENST00000455934.6:c.914+67del	ENSP00000392709.2:n.914+67del
ENST00000457011.5:c.524+67del	ENSP00000400976.1:n.524+67del
NM_001199981.1:c.764+67del	NP_001186910.1:n.764+67del
NM_001199982.1:c.539+67del	NP_001186911.1:n.539+67del
NM_001199983.1:c.701+67del	NP_001186912.1:n.701+67del
NM_001199984.1:c.914+67del	NP_001186913.1:n.914+67del
NM_005006.6:c.872+67del	NP_004997.4:n.872+67del
XM_017004188.2:c.113+67del	XP_016859677.1:n.113+67del
NM_001199981.2:c.764+67del	NP_001186910.1:n.764+67del
NM_001199982.2:c.539+67del	NP_001186911.1:n.539+67del
NM_001199983.2:c.701+67del	NP_001186912.1:n.701+67del
NM_005006.7:c.872+67del MANE Select	NP_004997.4:n.872+67del
NM_001199984.2:c.914+67del	NP_001186913.1:n.914+67del