Canonical Allele Identifier: CA350057578

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009715C>G (hg19) ; chr2:g.206144991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144991C>G , CM000664.2:g.206144991C>G	GRCh38
NC_000002.11:g.207009715C>G , CM000664.1:g.207009715C>G	GRCh37
NC_000002.10:g.206717960C>G	NCBI36
NG_009248.1:g.19473G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.773G>C MANE Select	ENSP00000233190.5:p.Gly258Ala
ENST00000233190.10:c.773G>C	ENSP00000233190.5:p.Gly258Ala
ENST00000423725.5:c.602G>C	ENSP00000397760.1:p.Gly201Ala
ENST00000432169.5:c.440G>C	ENSP00000409689.1:p.Gly147Ala
ENST00000440274.5:c.665G>C	ENSP00000409766.1:p.Gly222Ala
ENST00000449699.5:c.773G>C	ENSP00000399912.1:p.Gly258Ala
ENST00000455934.6:c.815G>C	ENSP00000392709.2:p.Gly272Ala
ENST00000457011.5:c.425G>C	ENSP00000400976.1:p.Gly142Ala
NM_001199981.1:c.665G>C	NP_001186910.1:p.Gly222Ala
NM_001199982.1:c.440G>C	NP_001186911.1:p.Gly147Ala
NM_001199983.1:c.602G>C	NP_001186912.1:p.Gly201Ala
NM_001199984.1:c.815G>C	NP_001186913.1:p.Gly272Ala
NM_005006.6:c.773G>C	NP_004997.4:p.Gly258Ala
XM_017004188.2:c.14G>C	XP_016859677.1:p.Gly5Ala
NM_001199981.2:c.665G>C	NP_001186910.1:p.Gly222Ala
NM_001199982.2:c.440G>C	NP_001186911.1:p.Gly147Ala
NM_001199983.2:c.602G>C	NP_001186912.1:p.Gly201Ala
NM_005006.7:c.773G>C MANE Select	NP_004997.4:p.Gly258Ala
NM_001199984.2:c.815G>C	NP_001186913.1:p.Gly272Ala