Canonical Allele Identifier: CA350057451

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009696G>T (hg19) ; chr2:g.206144972G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144972G>T , CM000664.2:g.206144972G>T	GRCh38
NC_000002.11:g.207009696G>T , CM000664.1:g.207009696G>T	GRCh37
NC_000002.10:g.206717941G>T	NCBI36
NG_009248.1:g.19492C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.792C>A MANE Select	ENSP00000233190.5:p.Ser264Arg
ENST00000233190.10:c.792C>A	ENSP00000233190.5:p.Ser264Arg
ENST00000423725.5:c.621C>A	ENSP00000397760.1:p.Ser207Arg
ENST00000432169.5:c.459C>A	ENSP00000409689.1:p.Ser153Arg
ENST00000440274.5:c.684C>A	ENSP00000409766.1:p.Ser228Arg
ENST00000449699.5:c.792C>A	ENSP00000399912.1:p.Ser264Arg
ENST00000455934.6:c.834C>A	ENSP00000392709.2:p.Ser278Arg
ENST00000457011.5:c.444C>A	ENSP00000400976.1:p.Ser148Arg
NM_001199981.1:c.684C>A	NP_001186910.1:p.Ser228Arg
NM_001199982.1:c.459C>A	NP_001186911.1:p.Ser153Arg
NM_001199983.1:c.621C>A	NP_001186912.1:p.Ser207Arg
NM_001199984.1:c.834C>A	NP_001186913.1:p.Ser278Arg
NM_005006.6:c.792C>A	NP_004997.4:p.Ser264Arg
XM_017004188.2:c.33C>A	XP_016859677.1:p.Ser11Arg
NM_001199981.2:c.684C>A	NP_001186910.1:p.Ser228Arg
NM_001199982.2:c.459C>A	NP_001186911.1:p.Ser153Arg
NM_001199983.2:c.621C>A	NP_001186912.1:p.Ser207Arg
NM_005006.7:c.792C>A MANE Select	NP_004997.4:p.Ser264Arg
NM_001199984.2:c.834C>A	NP_001186913.1:p.Ser278Arg