Canonical Allele Identifier: CA350056992

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009637T>C (hg19) ; chr2:g.206144913T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144913T>C , CM000664.2:g.206144913T>C	GRCh38
NC_000002.11:g.207009637T>C , CM000664.1:g.207009637T>C	GRCh37
NC_000002.10:g.206717882T>C	NCBI36
NG_009248.1:g.19551A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.851A>G MANE Select	ENSP00000233190.5:p.Glu284Gly
ENST00000233190.10:c.851A>G	ENSP00000233190.5:p.Glu284Gly
ENST00000423725.5:c.680A>G	ENSP00000397760.1:p.Glu227Gly
ENST00000432169.5:c.518A>G	ENSP00000409689.1:p.Glu173Gly
ENST00000440274.5:c.743A>G	ENSP00000409766.1:p.Glu248Gly
ENST00000449699.5:c.851A>G	ENSP00000399912.1:p.Glu284Gly
ENST00000455934.6:c.893A>G	ENSP00000392709.2:p.Glu298Gly
ENST00000457011.5:c.503A>G	ENSP00000400976.1:p.Glu168Gly
NM_001199981.1:c.743A>G	NP_001186910.1:p.Glu248Gly
NM_001199982.1:c.518A>G	NP_001186911.1:p.Glu173Gly
NM_001199983.1:c.680A>G	NP_001186912.1:p.Glu227Gly
NM_001199984.1:c.893A>G	NP_001186913.1:p.Glu298Gly
NM_005006.6:c.851A>G	NP_004997.4:p.Glu284Gly
XM_017004188.2:c.92A>G	XP_016859677.1:p.Glu31Gly
NM_001199981.2:c.743A>G	NP_001186910.1:p.Glu248Gly
NM_001199982.2:c.518A>G	NP_001186911.1:p.Glu173Gly
NM_001199983.2:c.680A>G	NP_001186912.1:p.Glu227Gly
NM_005006.7:c.851A>G MANE Select	NP_004997.4:p.Glu284Gly
NM_001199984.2:c.893A>G	NP_001186913.1:p.Glu298Gly