Canonical Allele Identifier: CA2662803777

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206144762-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144764del , CM000664.2:g.206144764del	GRCh38
NC_000002.11:g.207009488del , CM000664.1:g.207009488del	GRCh37
NC_000002.10:g.206717733del	NCBI36
NG_009248.1:g.19701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.872+129del MANE Select	ENSP00000233190.5:n.872+129del
ENST00000233190.10:c.872+129del	ENSP00000233190.5:n.872+129del
ENST00000423725.5:c.701+129del	ENSP00000397760.1:n.701+129del
ENST00000432169.5:c.539+129del	ENSP00000409689.1:n.539+129del
ENST00000440274.5:c.764+129del	ENSP00000409766.1:n.764+129del
ENST00000449699.5:c.872+129del	ENSP00000399912.1:n.872+129del
ENST00000455934.6:c.914+129del	ENSP00000392709.2:n.914+129del
ENST00000457011.5:c.524+129del	ENSP00000400976.1:n.524+129del
NM_001199981.1:c.764+129del	NP_001186910.1:n.764+129del
NM_001199982.1:c.539+129del	NP_001186911.1:n.539+129del
NM_001199983.1:c.701+129del	NP_001186912.1:n.701+129del
NM_001199984.1:c.914+129del	NP_001186913.1:n.914+129del
NM_005006.6:c.872+129del	NP_004997.4:n.872+129del
XM_017004188.2:c.113+129del	XP_016859677.1:n.113+129del
NM_001199981.2:c.764+129del	NP_001186910.1:n.764+129del
NM_001199982.2:c.539+129del	NP_001186911.1:n.539+129del
NM_001199983.2:c.701+129del	NP_001186912.1:n.701+129del
NM_005006.7:c.872+129del MANE Select	NP_004997.4:n.872+129del
NM_001199984.2:c.914+129del	NP_001186913.1:n.914+129del