Canonical Allele Identifier: CA475416852

Gene: NDUFV1

Linked Data

• dbSNP Id: rs1295112014
• gnomAD v2: 11-67378911-G-A
• gnomAD v4: 11-67611440-G-A
• MyVariant Identifiers: chr11:g.67378911G>A (hg19) ; chr11:g.67611440G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611440G>A , CM000673.2:g.67611440G>A	GRCh38
NC_000011.9:g.67378911G>A , CM000673.1:g.67378911G>A	GRCh37
NC_000011.8:g.67135487G>A	NCBI36
NG_013353.1:g.9589G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.951G>A MANE Select	ENSP00000322450.6:p.Val317=
ENST00000647561.1:c.951G>A	ENSP00000497587.1:p.Val317=
ENST00000322776.10:c.951G>A	ENSP00000322450.6:p.Val317=
ENST00000415352.6:c.930G>A	ENSP00000395368.2:p.Val310=
ENST00000526169.1:n.656-82G>A
ENST00000526770.5:n.1234G>A
ENST00000527355.5:c.240G>A	ENSP00000432637.1:p.Val80=
ENST00000527923.1:n.293G>A
ENST00000529927.5:c.924G>A	ENSP00000436766.1:p.Val308=
ENST00000532303.5:c.648G>A	ENSP00000432015.1:p.Val216=
ENST00000533919.5:c.392-37G>A	ENSP00000435199.1:n.392-37G>A
NM_001166102.1:c.924G>A	NP_001159574.1:p.Val308=
NM_007103.3:c.951G>A	NP_009034.2:p.Val317=
NM_001166102.2:c.924G>A	NP_001159574.1:p.Val308=
NM_007103.4:c.951G>A MANE Select	NP_009034.2:p.Val317=