Canonical Allele Identifier: CA381540953

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378982C>G (hg19) ; chr11:g.67611511C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611511C>G , CM000673.2:g.67611511C>G	GRCh38
NC_000011.9:g.67378982C>G , CM000673.1:g.67378982C>G	GRCh37
NC_000011.8:g.67135558C>G	NCBI36
NG_013353.1:g.9660C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.1022C>G MANE Select	ENSP00000322450.6:p.Ala341Gly
ENST00000647561.1:c.1022C>G	ENSP00000497587.1:p.Ala341Gly
ENST00000322776.10:c.1022C>G	ENSP00000322450.6:p.Ala341Gly
ENST00000415352.6:c.1001C>G	ENSP00000395368.2:p.Ala334Gly
ENST00000526169.1:n.656-11C>G
ENST00000526770.5:n.1305C>G
ENST00000527355.5:c.311C>G	ENSP00000432637.1:p.Ala104Gly
ENST00000527923.1:n.364C>G
ENST00000529927.5:c.995C>G	ENSP00000436766.1:p.Ala332Gly
ENST00000532303.5:c.719C>G	ENSP00000432015.1:p.Ala240Gly
ENST00000533919.5:c.426C>G	ENSP00000435199.1:n.426C>G
NM_001166102.1:c.995C>G	NP_001159574.1:p.Ala332Gly
NM_007103.3:c.1022C>G	NP_009034.2:p.Ala341Gly
NM_001166102.2:c.995C>G	NP_001159574.1:p.Ala332Gly
NM_007103.4:c.1022C>G MANE Select	NP_009034.2:p.Ala341Gly