Canonical Allele Identifier: CA763755740

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1488103862
• gnomAD v3: 2-206144605-C-T
• gnomAD v4: 2-206144605-C-T
• MyVariant Identifiers: chr2:g.207009329C>T (hg19) ; chr2:g.206144605C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144605C>T , CM000664.2:g.206144605C>T	GRCh38
NC_000002.11:g.207009329C>T , CM000664.1:g.207009329C>T	GRCh37
NC_000002.10:g.206717574C>T	NCBI36
NG_009248.1:g.19859G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.872+287G>A MANE Select	ENSP00000233190.5:n.872+287G>A
ENST00000233190.10:c.872+287G>A	ENSP00000233190.5:n.872+287G>A
ENST00000423725.5:c.701+287G>A	ENSP00000397760.1:n.701+287G>A
ENST00000432169.5:c.539+287G>A	ENSP00000409689.1:n.539+287G>A
ENST00000440274.5:c.764+287G>A	ENSP00000409766.1:n.764+287G>A
ENST00000449699.5:c.872+287G>A	ENSP00000399912.1:n.872+287G>A
ENST00000455934.6:c.914+287G>A	ENSP00000392709.2:n.914+287G>A
ENST00000457011.5:c.524+287G>A	ENSP00000400976.1:n.524+287G>A
NM_001199981.1:c.764+287G>A	NP_001186910.1:n.764+287G>A
NM_001199982.1:c.539+287G>A	NP_001186911.1:n.539+287G>A
NM_001199983.1:c.701+287G>A	NP_001186912.1:n.701+287G>A
NM_001199984.1:c.914+287G>A	NP_001186913.1:n.914+287G>A
NM_005006.6:c.872+287G>A	NP_004997.4:n.872+287G>A
XM_017004188.2:c.113+287G>A	XP_016859677.1:n.113+287G>A
NM_001199981.2:c.764+287G>A	NP_001186910.1:n.764+287G>A
NM_001199982.2:c.539+287G>A	NP_001186911.1:n.539+287G>A
NM_001199983.2:c.701+287G>A	NP_001186912.1:n.701+287G>A
NM_005006.7:c.872+287G>A MANE Select	NP_004997.4:n.872+287G>A
NM_001199984.2:c.914+287G>A	NP_001186913.1:n.914+287G>A