Canonical Allele Identifier: CA350057609

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009722C>G (hg19) ; chr2:g.206144998C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144998C>G , CM000664.2:g.206144998C>G	GRCh38
NC_000002.11:g.207009722C>G , CM000664.1:g.207009722C>G	GRCh37
NC_000002.10:g.206717967C>G	NCBI36
NG_009248.1:g.19466G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.766G>C MANE Select	ENSP00000233190.5:p.Ala256Pro
ENST00000233190.10:c.766G>C	ENSP00000233190.5:p.Ala256Pro
ENST00000423725.5:c.595G>C	ENSP00000397760.1:p.Ala199Pro
ENST00000432169.5:c.433G>C	ENSP00000409689.1:p.Ala145Pro
ENST00000440274.5:c.658G>C	ENSP00000409766.1:p.Ala220Pro
ENST00000449699.5:c.766G>C	ENSP00000399912.1:p.Ala256Pro
ENST00000455934.6:c.808G>C	ENSP00000392709.2:p.Ala270Pro
ENST00000457011.5:c.418G>C	ENSP00000400976.1:p.Ala140Pro
NM_001199981.1:c.658G>C	NP_001186910.1:p.Ala220Pro
NM_001199982.1:c.433G>C	NP_001186911.1:p.Ala145Pro
NM_001199983.1:c.595G>C	NP_001186912.1:p.Ala199Pro
NM_001199984.1:c.808G>C	NP_001186913.1:p.Ala270Pro
NM_005006.6:c.766G>C	NP_004997.4:p.Ala256Pro
XM_017004188.2:c.7G>C	XP_016859677.1:p.Ala3Pro
NM_001199981.2:c.658G>C	NP_001186910.1:p.Ala220Pro
NM_001199982.2:c.433G>C	NP_001186911.1:p.Ala145Pro
NM_001199983.2:c.595G>C	NP_001186912.1:p.Ala199Pro
NM_005006.7:c.766G>C MANE Select	NP_004997.4:p.Ala256Pro
NM_001199984.2:c.808G>C	NP_001186913.1:p.Ala270Pro