Canonical Allele Identifier: CA381536355

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377850A>G (hg19) ; chr11:g.67610379A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610379A>G , CM000673.2:g.67610379A>G	GRCh38
NC_000011.9:g.67377850A>G , CM000673.1:g.67377850A>G	GRCh37
NC_000011.8:g.67134426A>G	NCBI36
NG_013353.1:g.8528A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.511-2A>G MANE Select	ENSP00000322450.6:n.511-2A>G
ENST00000647561.1:c.511-2A>G	ENSP00000497587.1:n.511-2A>G
ENST00000322776.10:c.511-2A>G	ENSP00000322450.6:n.511-2A>G
ENST00000415352.6:c.490-2A>G	ENSP00000395368.2:n.490-2A>G
ENST00000526169.1:n.253-2A>G
ENST00000526770.5:n.370-2A>G
ENST00000529867.5:c.475-2A>G	ENSP00000434438.1:n.475-2A>G
ENST00000529927.5:c.484-2A>G	ENSP00000436766.1:n.484-2A>G
ENST00000530638.1:c.394-2A>G	ENSP00000436936.1:n.394-2A>G
ENST00000532244.5:c.208-2A>G	ENSP00000435202.1:n.208-2A>G
ENST00000532303.5:c.208-2A>G	ENSP00000432015.1:n.208-2A>G
ENST00000532343.5:c.208-2A>G	ENSP00000431751.1:n.208-2A>G
ENST00000533075.5:c.490-2A>G	ENSP00000437267.1:n.490-2A>G
NM_001166102.1:c.484-2A>G	NP_001159574.1:n.484-2A>G
NM_007103.3:c.511-2A>G	NP_009034.2:n.511-2A>G
NM_001166102.2:c.484-2A>G	NP_001159574.1:n.484-2A>G
NM_007103.4:c.511-2A>G MANE Select	NP_009034.2:n.511-2A>G