Canonical Allele Identifier: CA350057379

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206144959-C-A
• MyVariant Identifiers: chr2:g.207009683C>A (hg19) ; chr2:g.206144959C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144959C>A , CM000664.2:g.206144959C>A	GRCh38
NC_000002.11:g.207009683C>A , CM000664.1:g.207009683C>A	GRCh37
NC_000002.10:g.206717928C>A	NCBI36
NG_009248.1:g.19505G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.805G>T MANE Select	ENSP00000233190.5:p.Glu269Ter
ENST00000233190.10:c.805G>T	ENSP00000233190.5:p.Glu269Ter
ENST00000423725.5:c.634G>T	ENSP00000397760.1:p.Glu212Ter
ENST00000432169.5:c.472G>T	ENSP00000409689.1:p.Glu158Ter
ENST00000440274.5:c.697G>T	ENSP00000409766.1:p.Glu233Ter
ENST00000449699.5:c.805G>T	ENSP00000399912.1:p.Glu269Ter
ENST00000455934.6:c.847G>T	ENSP00000392709.2:p.Glu283Ter
ENST00000457011.5:c.457G>T	ENSP00000400976.1:p.Glu153Ter
NM_001199981.1:c.697G>T	NP_001186910.1:p.Glu233Ter
NM_001199982.1:c.472G>T	NP_001186911.1:p.Glu158Ter
NM_001199983.1:c.634G>T	NP_001186912.1:p.Glu212Ter
NM_001199984.1:c.847G>T	NP_001186913.1:p.Glu283Ter
NM_005006.6:c.805G>T	NP_004997.4:p.Glu269Ter
XM_017004188.2:c.46G>T	XP_016859677.1:p.Glu16Ter
NM_001199981.2:c.697G>T	NP_001186910.1:p.Glu233Ter
NM_001199982.2:c.472G>T	NP_001186911.1:p.Glu158Ter
NM_001199983.2:c.634G>T	NP_001186912.1:p.Glu212Ter
NM_005006.7:c.805G>T MANE Select	NP_004997.4:p.Glu269Ter
NM_001199984.2:c.847G>T	NP_001186913.1:p.Glu283Ter