Canonical Allele Identifier: CA350057275

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009669A>C (hg19) ; chr2:g.206144945A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144945A>C , CM000664.2:g.206144945A>C	GRCh38
NC_000002.11:g.207009669A>C , CM000664.1:g.207009669A>C	GRCh37
NC_000002.10:g.206717914A>C	NCBI36
NG_009248.1:g.19519T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.819T>G MANE Select	ENSP00000233190.5:p.Ile273Met
ENST00000233190.10:c.819T>G	ENSP00000233190.5:p.Ile273Met
ENST00000423725.5:c.648T>G	ENSP00000397760.1:p.Ile216Met
ENST00000432169.5:c.486T>G	ENSP00000409689.1:p.Ile162Met
ENST00000440274.5:c.711T>G	ENSP00000409766.1:p.Ile237Met
ENST00000449699.5:c.819T>G	ENSP00000399912.1:p.Ile273Met
ENST00000455934.6:c.861T>G	ENSP00000392709.2:p.Ile287Met
ENST00000457011.5:c.471T>G	ENSP00000400976.1:p.Ile157Met
NM_001199981.1:c.711T>G	NP_001186910.1:p.Ile237Met
NM_001199982.1:c.486T>G	NP_001186911.1:p.Ile162Met
NM_001199983.1:c.648T>G	NP_001186912.1:p.Ile216Met
NM_001199984.1:c.861T>G	NP_001186913.1:p.Ile287Met
NM_005006.6:c.819T>G	NP_004997.4:p.Ile273Met
XM_017004188.2:c.60T>G	XP_016859677.1:p.Ile20Met
NM_001199981.2:c.711T>G	NP_001186910.1:p.Ile237Met
NM_001199982.2:c.486T>G	NP_001186911.1:p.Ile162Met
NM_001199983.2:c.648T>G	NP_001186912.1:p.Ile216Met
NM_005006.7:c.819T>G MANE Select	NP_004997.4:p.Ile273Met
NM_001199984.2:c.861T>G	NP_001186913.1:p.Ile287Met