Canonical Allele Identifier: CA430942881

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206127809-T-C
• MyVariant Identifiers: chr2:g.206992533T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127809T>C , CM000664.2:g.206127809T>C	GRCh38
NC_000002.11:g.206992533T>C , CM000664.1:g.206992533T>C	GRCh37
NC_000002.10:g.206700778T>C	NCBI36
NG_009248.1:g.36655A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1872A>G MANE Select	ENSP00000233190.5:p.Arg624=
ENST00000233190.10:c.1872A>G	ENSP00000233190.5:p.Arg624=
ENST00000423725.5:c.1701A>G	ENSP00000397760.1:p.Arg567=
ENST00000432169.5:c.1539A>G	ENSP00000409689.1:p.Arg513=
ENST00000440274.5:c.1764A>G	ENSP00000409766.1:p.Arg588=
ENST00000449699.5:c.1872A>G	ENSP00000399912.1:p.Arg624=
ENST00000455934.6:c.1914A>G	ENSP00000392709.2:p.Arg638=
ENST00000457011.5:c.1524A>G	ENSP00000400976.1:p.Arg508=
ENST00000498520.1:n.344A>G
NM_001199981.1:c.1764A>G	NP_001186910.1:p.Arg588=
NM_001199982.1:c.1539A>G	NP_001186911.1:p.Arg513=
NM_001199983.1:c.1701A>G	NP_001186912.1:p.Arg567=
NM_001199984.1:c.1914A>G	NP_001186913.1:p.Arg638=
NM_005006.6:c.1872A>G	NP_004997.4:p.Arg624=
XM_017004188.2:c.1113A>G	XP_016859677.1:p.Arg371=
NM_001199981.2:c.1764A>G	NP_001186910.1:p.Arg588=
NM_001199982.2:c.1539A>G	NP_001186911.1:p.Arg513=
NM_001199983.2:c.1701A>G	NP_001186912.1:p.Arg567=
NM_005006.7:c.1872A>G MANE Select	NP_004997.4:p.Arg624=
NM_001199984.2:c.1914A>G	NP_001186913.1:p.Arg638=