Canonical Allele Identifier: CA350056229

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009616C>A (hg19) ; chr2:g.206144892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144892C>A , CM000664.2:g.206144892C>A	GRCh38
NC_000002.11:g.207009616C>A , CM000664.1:g.207009616C>A	GRCh37
NC_000002.10:g.206717861C>A	NCBI36
NG_009248.1:g.19572G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.872G>T MANE Select	ENSP00000233190.5:p.Arg291Ile
ENST00000233190.10:c.872G>T	ENSP00000233190.5:p.Arg291Ile
ENST00000423725.5:c.701G>T	ENSP00000397760.1:p.Arg234Ile
ENST00000432169.5:c.539G>T	ENSP00000409689.1:p.Arg180Ile
ENST00000440274.5:c.764G>T	ENSP00000409766.1:p.Arg255Ile
ENST00000449699.5:c.872G>T	ENSP00000399912.1:p.Arg291Ile
ENST00000455934.6:c.914G>T	ENSP00000392709.2:p.Arg305Ile
ENST00000457011.5:c.524G>T	ENSP00000400976.1:p.Arg175Ile
NM_001199981.1:c.764G>T	NP_001186910.1:p.Arg255Ile
NM_001199982.1:c.539G>T	NP_001186911.1:p.Arg180Ile
NM_001199983.1:c.701G>T	NP_001186912.1:p.Arg234Ile
NM_001199984.1:c.914G>T	NP_001186913.1:p.Arg305Ile
NM_005006.6:c.872G>T	NP_004997.4:p.Arg291Ile
XM_017004188.2:c.113G>T	XP_016859677.1:p.Arg38Ile
NM_001199981.2:c.764G>T	NP_001186910.1:p.Arg255Ile
NM_001199982.2:c.539G>T	NP_001186911.1:p.Arg180Ile
NM_001199983.2:c.701G>T	NP_001186912.1:p.Arg234Ile
NM_005006.7:c.872G>T MANE Select	NP_004997.4:p.Arg291Ile
NM_001199984.2:c.914G>T	NP_001186913.1:p.Arg305Ile