Canonical Allele Identifier: CA350057411

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1692101775
• MyVariant Identifiers: chr2:g.207009688G>C (hg19) ; chr2:g.206144964G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144964G>C , CM000664.2:g.206144964G>C	GRCh38
NC_000002.11:g.207009688G>C , CM000664.1:g.207009688G>C	GRCh37
NC_000002.10:g.206717933G>C	NCBI36
NG_009248.1:g.19500C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.800C>G MANE Select	ENSP00000233190.5:p.Thr267Ser
ENST00000233190.10:c.800C>G	ENSP00000233190.5:p.Thr267Ser
ENST00000423725.5:c.629C>G	ENSP00000397760.1:p.Thr210Ser
ENST00000432169.5:c.467C>G	ENSP00000409689.1:p.Thr156Ser
ENST00000440274.5:c.692C>G	ENSP00000409766.1:p.Thr231Ser
ENST00000449699.5:c.800C>G	ENSP00000399912.1:p.Thr267Ser
ENST00000455934.6:c.842C>G	ENSP00000392709.2:p.Thr281Ser
ENST00000457011.5:c.452C>G	ENSP00000400976.1:p.Thr151Ser
NM_001199981.1:c.692C>G	NP_001186910.1:p.Thr231Ser
NM_001199982.1:c.467C>G	NP_001186911.1:p.Thr156Ser
NM_001199983.1:c.629C>G	NP_001186912.1:p.Thr210Ser
NM_001199984.1:c.842C>G	NP_001186913.1:p.Thr281Ser
NM_005006.6:c.800C>G	NP_004997.4:p.Thr267Ser
XM_017004188.2:c.41C>G	XP_016859677.1:p.Thr14Ser
NM_001199981.2:c.692C>G	NP_001186910.1:p.Thr231Ser
NM_001199982.2:c.467C>G	NP_001186911.1:p.Thr156Ser
NM_001199983.2:c.629C>G	NP_001186912.1:p.Thr210Ser
NM_005006.7:c.800C>G MANE Select	NP_004997.4:p.Thr267Ser
NM_001199984.2:c.842C>G	NP_001186913.1:p.Thr281Ser