Canonical Allele Identifier: CA350057204

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009659T>C (hg19) ; chr2:g.206144935T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144935T>C , CM000664.2:g.206144935T>C	GRCh38
NC_000002.11:g.207009659T>C , CM000664.1:g.207009659T>C	GRCh37
NC_000002.10:g.206717904T>C	NCBI36
NG_009248.1:g.19529A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.829A>G MANE Select	ENSP00000233190.5:p.Met277Val
ENST00000233190.10:c.829A>G	ENSP00000233190.5:p.Met277Val
ENST00000423725.5:c.658A>G	ENSP00000397760.1:p.Met220Val
ENST00000432169.5:c.496A>G	ENSP00000409689.1:p.Met166Val
ENST00000440274.5:c.721A>G	ENSP00000409766.1:p.Met241Val
ENST00000449699.5:c.829A>G	ENSP00000399912.1:p.Met277Val
ENST00000455934.6:c.871A>G	ENSP00000392709.2:p.Met291Val
ENST00000457011.5:c.481A>G	ENSP00000400976.1:p.Met161Val
NM_001199981.1:c.721A>G	NP_001186910.1:p.Met241Val
NM_001199982.1:c.496A>G	NP_001186911.1:p.Met166Val
NM_001199983.1:c.658A>G	NP_001186912.1:p.Met220Val
NM_001199984.1:c.871A>G	NP_001186913.1:p.Met291Val
NM_005006.6:c.829A>G	NP_004997.4:p.Met277Val
XM_017004188.2:c.70A>G	XP_016859677.1:p.Met24Val
NM_001199981.2:c.721A>G	NP_001186910.1:p.Met241Val
NM_001199982.2:c.496A>G	NP_001186911.1:p.Met166Val
NM_001199983.2:c.658A>G	NP_001186912.1:p.Met220Val
NM_005006.7:c.829A>G MANE Select	NP_004997.4:p.Met277Val
NM_001199984.2:c.871A>G	NP_001186913.1:p.Met291Val