Canonical Allele Identifier: CA2070663

Gene: NDUFS1

Linked Data

• dbSNP Id: rs747821264
• ExAC: 2:207009747 C / T
• gnomAD v2: 2-207009747-C-T
• gnomAD v4: 2-206145023-C-T
• MyVariant Identifiers: chr2:g.207009747C>T (hg19) ; chr2:g.206145023C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145023C>T , CM000664.2:g.206145023C>T	GRCh38
NC_000002.11:g.207009747C>T , CM000664.1:g.207009747C>T	GRCh37
NC_000002.10:g.206717992C>T	NCBI36
NG_009248.1:g.19441G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.741G>A MANE Select	ENSP00000233190.5:p.Lys247=
ENST00000233190.10:c.741G>A	ENSP00000233190.5:p.Lys247=
ENST00000423725.5:c.570G>A	ENSP00000397760.1:p.Lys190=
ENST00000432169.5:c.408G>A	ENSP00000409689.1:p.Lys136=
ENST00000440274.5:c.633G>A	ENSP00000409766.1:p.Lys211=
ENST00000449699.5:c.741G>A	ENSP00000399912.1:p.Lys247=
ENST00000455934.6:c.783G>A	ENSP00000392709.2:p.Lys261=
ENST00000457011.5:c.393G>A	ENSP00000400976.1:p.Lys131=
NM_001199981.1:c.633G>A	NP_001186910.1:p.Lys211=
NM_001199982.1:c.408G>A	NP_001186911.1:p.Lys136=
NM_001199983.1:c.570G>A	NP_001186912.1:p.Lys190=
NM_001199984.1:c.783G>A	NP_001186913.1:p.Lys261=
NM_005006.6:c.741G>A	NP_004997.4:p.Lys247=
XM_017004188.2:c.-19G>A	XP_016859677.1:n.-19G>A
NM_001199981.2:c.633G>A	NP_001186910.1:p.Lys211=
NM_001199982.2:c.408G>A	NP_001186911.1:p.Lys136=
NM_001199983.2:c.570G>A	NP_001186912.1:p.Lys190=
NM_005006.7:c.741G>A MANE Select	NP_004997.4:p.Lys247=
NM_001199984.2:c.783G>A	NP_001186913.1:p.Lys261=