Canonical Allele Identifier: CA2614649015

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67611313-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611313G>T , CM000673.2:g.67611313G>T	GRCh38
NC_000011.9:g.67378784G>T , CM000673.1:g.67378784G>T	GRCh37
NC_000011.8:g.67135360G>T	NCBI36
NG_013353.1:g.9462G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.914-90G>T MANE Select	ENSP00000322450.6:n.914-90G>T
ENST00000647561.1:c.914-90G>T	ENSP00000497587.1:n.914-90G>T
ENST00000322776.10:c.914-90G>T	ENSP00000322450.6:n.914-90G>T
ENST00000415352.6:c.893-90G>T	ENSP00000395368.2:n.893-90G>T
ENST00000526169.1:n.655+106G>T
ENST00000526770.5:n.1197-90G>T
ENST00000527355.5:c.203-90G>T	ENSP00000432637.1:n.203-90G>T
ENST00000527923.1:n.166G>T
ENST00000529927.5:c.887-90G>T	ENSP00000436766.1:n.887-90G>T
ENST00000532303.5:c.611-90G>T	ENSP00000432015.1:n.611-90G>T
ENST00000533919.5:c.391+106G>T	ENSP00000435199.1:n.391+106G>T
NM_001166102.1:c.887-90G>T	NP_001159574.1:n.887-90G>T
NM_007103.3:c.914-90G>T	NP_009034.2:n.914-90G>T
NM_001166102.2:c.887-90G>T	NP_001159574.1:n.887-90G>T
NM_007103.4:c.914-90G>T MANE Select	NP_009034.2:n.914-90G>T