Canonical Allele Identifier: CA763787306

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1318743372
• MyVariant Identifiers: chr2:g.206988008_206988009insTCCCTCATTCCAAGGGAA (hg19) ; chr2:g.206123284_206123285insTCCCTCATTCCAAGGGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206123301_206123302insATCCCTCATTCCAAGGGA , CM000664.2:g.206123301_206123302insATCCCTCATTCCAAGGGA	GRCh38
NC_000002.11:g.206988025_206988026insATCCCTCATTCCAAGGGA , CM000664.1:g.206988025_206988026insATCCCTCATTCCAAGGGA	GRCh37
NC_000002.10:g.206696270_206696271insATCCCTCATTCCAAGGGA	NCBI36
NG_009248.1:g.41179_41180insTTCCCTTGGAATGAGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.*900_*901insTTCCCTTGGAATGAGGGA MANE Select	ENSP00000233190.5:n.*900_*901insTTCCCTTGGAATGAGGGA
ENST00000233190.10:c.*900_*901insTTCCCTTGGAATGAGGGA	ENSP00000233190.5:n.*900_*901insTTCCCTTGGAATGAGGGA
ENST00000455934.6:c.*900_*901insTTCCCTTGGAATGAGGGA	ENSP00000392709.2:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199981.1:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186910.1:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199982.1:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186911.1:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199983.1:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186912.1:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199984.1:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186913.1:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_005006.6:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_004997.4:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199981.2:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186910.1:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199982.2:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186911.1:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199983.2:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186912.1:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_005006.7:c.*900_*901insTTCCCTTGGAATGAGGGA MANE Select	NP_004997.4:n.*900_*901insTTCCCTTGGAATGAGGGA
NM_001199984.2:c.*900_*901insTTCCCTTGGAATGAGGGA	NP_001186913.1:n.*900_*901insTTCCCTTGGAATGAGGGA