Canonical Allele Identifier: CA350057516

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009706A>T (hg19) ; chr2:g.206144982A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144982A>T , CM000664.2:g.206144982A>T	GRCh38
NC_000002.11:g.207009706A>T , CM000664.1:g.207009706A>T	GRCh37
NC_000002.10:g.206717951A>T	NCBI36
NG_009248.1:g.19482T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.782T>A MANE Select	ENSP00000233190.5:p.Ile261Asn
ENST00000233190.10:c.782T>A	ENSP00000233190.5:p.Ile261Asn
ENST00000423725.5:c.611T>A	ENSP00000397760.1:p.Ile204Asn
ENST00000432169.5:c.449T>A	ENSP00000409689.1:p.Ile150Asn
ENST00000440274.5:c.674T>A	ENSP00000409766.1:p.Ile225Asn
ENST00000449699.5:c.782T>A	ENSP00000399912.1:p.Ile261Asn
ENST00000455934.6:c.824T>A	ENSP00000392709.2:p.Ile275Asn
ENST00000457011.5:c.434T>A	ENSP00000400976.1:p.Ile145Asn
NM_001199981.1:c.674T>A	NP_001186910.1:p.Ile225Asn
NM_001199982.1:c.449T>A	NP_001186911.1:p.Ile150Asn
NM_001199983.1:c.611T>A	NP_001186912.1:p.Ile204Asn
NM_001199984.1:c.824T>A	NP_001186913.1:p.Ile275Asn
NM_005006.6:c.782T>A	NP_004997.4:p.Ile261Asn
XM_017004188.2:c.23T>A	XP_016859677.1:p.Ile8Asn
NM_001199981.2:c.674T>A	NP_001186910.1:p.Ile225Asn
NM_001199982.2:c.449T>A	NP_001186911.1:p.Ile150Asn
NM_001199983.2:c.611T>A	NP_001186912.1:p.Ile204Asn
NM_005006.7:c.782T>A MANE Select	NP_004997.4:p.Ile261Asn
NM_001199984.2:c.824T>A	NP_001186913.1:p.Ile275Asn