Canonical Allele Identifier: CA381540777

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378940T>G (hg19) ; chr11:g.67611469T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611469T>G , CM000673.2:g.67611469T>G	GRCh38
NC_000011.9:g.67378940T>G , CM000673.1:g.67378940T>G	GRCh37
NC_000011.8:g.67135516T>G	NCBI36
NG_013353.1:g.9618T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.980T>G MANE Select	ENSP00000322450.6:p.Ile327Ser
ENST00000647561.1:c.980T>G	ENSP00000497587.1:p.Ile327Ser
ENST00000322776.10:c.980T>G	ENSP00000322450.6:p.Ile327Ser
ENST00000415352.6:c.959T>G	ENSP00000395368.2:p.Ile320Ser
ENST00000526169.1:n.656-53T>G
ENST00000526770.5:n.1263T>G
ENST00000527355.5:c.269T>G	ENSP00000432637.1:p.Ile90Ser
ENST00000527923.1:n.322T>G
ENST00000529927.5:c.953T>G	ENSP00000436766.1:p.Ile318Ser
ENST00000532303.5:c.677T>G	ENSP00000432015.1:p.Ile226Ser
ENST00000533919.5:c.392-8T>G	ENSP00000435199.1:n.392-8T>G
NM_001166102.1:c.953T>G	NP_001159574.1:p.Ile318Ser
NM_007103.3:c.980T>G	NP_009034.2:p.Ile327Ser
NM_001166102.2:c.953T>G	NP_001159574.1:p.Ile318Ser
NM_007103.4:c.980T>G MANE Select	NP_009034.2:p.Ile327Ser