Canonical Allele Identifier: CA475511021

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67611908-G-T
• MyVariant Identifiers: chr11:g.67379379G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611908G>T , CM000673.2:g.67611908G>T	GRCh38
NC_000011.9:g.67379379G>T , CM000673.1:g.67379379G>T	GRCh37
NC_000011.8:g.67135955G>T	NCBI36
NG_013353.1:g.10057G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1092G>T MANE Select	ENSP00000322450.6:p.Val364=
ENST00000647561.1:c.1092G>T	ENSP00000497587.1:p.Val364=
ENST00000322776.10:c.1092G>T	ENSP00000322450.6:p.Val364=
ENST00000415352.6:c.1071G>T	ENSP00000395368.2:p.Val357=
ENST00000526169.1:n.715G>T
ENST00000526770.5:n.1375G>T
ENST00000527355.5:c.370-212G>T	ENSP00000432637.1:n.370-212G>T
ENST00000527923.1:n.434G>T
ENST00000529927.5:c.1065G>T	ENSP00000436766.1:p.Val355=
ENST00000531250.1:n.356G>T
ENST00000532303.5:c.789G>T	ENSP00000432015.1:p.Val263=
ENST00000533919.5:c.496G>T	ENSP00000435199.1:n.496G>T
ENST00000534352.1:n.190G>T
NM_001166102.1:c.1065G>T	NP_001159574.1:p.Val355=
NM_007103.3:c.1092G>T	NP_009034.2:p.Val364=
NM_001166102.2:c.1065G>T	NP_001159574.1:p.Val355=
NM_007103.4:c.1092G>T MANE Select	NP_009034.2:p.Val364=