Canonical Allele Identifier: CA350057677

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009731C>A (hg19) ; chr2:g.206145007C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145007C>A , CM000664.2:g.206145007C>A	GRCh38
NC_000002.11:g.207009731C>A , CM000664.1:g.207009731C>A	GRCh37
NC_000002.10:g.206717976C>A	NCBI36
NG_009248.1:g.19457G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.757G>T MANE Select	ENSP00000233190.5:p.Val253Leu
ENST00000233190.10:c.757G>T	ENSP00000233190.5:p.Val253Leu
ENST00000423725.5:c.586G>T	ENSP00000397760.1:p.Val196Leu
ENST00000432169.5:c.424G>T	ENSP00000409689.1:p.Val142Leu
ENST00000440274.5:c.649G>T	ENSP00000409766.1:p.Val217Leu
ENST00000449699.5:c.757G>T	ENSP00000399912.1:p.Val253Leu
ENST00000455934.6:c.799G>T	ENSP00000392709.2:p.Val267Leu
ENST00000457011.5:c.409G>T	ENSP00000400976.1:p.Val137Leu
NM_001199981.1:c.649G>T	NP_001186910.1:p.Val217Leu
NM_001199982.1:c.424G>T	NP_001186911.1:p.Val142Leu
NM_001199983.1:c.586G>T	NP_001186912.1:p.Val196Leu
NM_001199984.1:c.799G>T	NP_001186913.1:p.Val267Leu
NM_005006.6:c.757G>T	NP_004997.4:p.Val253Leu
XM_017004188.2:c.-3G>T	XP_016859677.1:n.-3G>T
NM_001199981.2:c.649G>T	NP_001186910.1:p.Val217Leu
NM_001199982.2:c.424G>T	NP_001186911.1:p.Val142Leu
NM_001199983.2:c.586G>T	NP_001186912.1:p.Val196Leu
NM_005006.7:c.757G>T MANE Select	NP_004997.4:p.Val253Leu
NM_001199984.2:c.799G>T	NP_001186913.1:p.Val267Leu