Canonical Allele Identifier: CA350057244

Gene: NDUFS1

Linked Data

• COSMIC: COSM3990998
• MyVariant Identifiers: chr2:g.207009665G>A (hg19) ; chr2:g.206144941G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144941G>A , CM000664.2:g.206144941G>A	GRCh38
NC_000002.11:g.207009665G>A , CM000664.1:g.207009665G>A	GRCh37
NC_000002.10:g.206717910G>A	NCBI36
NG_009248.1:g.19523C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.823C>T MANE Select	ENSP00000233190.5:p.Pro275Ser
ENST00000233190.10:c.823C>T	ENSP00000233190.5:p.Pro275Ser
ENST00000423725.5:c.652C>T	ENSP00000397760.1:p.Pro218Ser
ENST00000432169.5:c.490C>T	ENSP00000409689.1:p.Pro164Ser
ENST00000440274.5:c.715C>T	ENSP00000409766.1:p.Pro239Ser
ENST00000449699.5:c.823C>T	ENSP00000399912.1:p.Pro275Ser
ENST00000455934.6:c.865C>T	ENSP00000392709.2:p.Pro289Ser
ENST00000457011.5:c.475C>T	ENSP00000400976.1:p.Pro159Ser
NM_001199981.1:c.715C>T	NP_001186910.1:p.Pro239Ser
NM_001199982.1:c.490C>T	NP_001186911.1:p.Pro164Ser
NM_001199983.1:c.652C>T	NP_001186912.1:p.Pro218Ser
NM_001199984.1:c.865C>T	NP_001186913.1:p.Pro289Ser
NM_005006.6:c.823C>T	NP_004997.4:p.Pro275Ser
XM_017004188.2:c.64C>T	XP_016859677.1:p.Pro22Ser
NM_001199981.2:c.715C>T	NP_001186910.1:p.Pro239Ser
NM_001199982.2:c.490C>T	NP_001186911.1:p.Pro164Ser
NM_001199983.2:c.652C>T	NP_001186912.1:p.Pro218Ser
NM_005006.7:c.823C>T MANE Select	NP_004997.4:p.Pro275Ser
NM_001199984.2:c.865C>T	NP_001186913.1:p.Pro289Ser