Canonical Allele Identifier: CA381540469

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67611415-G-A
• MyVariant Identifiers: chr11:g.67378886G>A (hg19) ; chr11:g.67611415G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611415G>A , CM000673.2:g.67611415G>A	GRCh38
NC_000011.9:g.67378886G>A , CM000673.1:g.67378886G>A	GRCh37
NC_000011.8:g.67135462G>A	NCBI36
NG_013353.1:g.9564G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.926G>A MANE Select	ENSP00000322450.6:p.Gly309Asp
ENST00000647561.1:c.926G>A	ENSP00000497587.1:p.Gly309Asp
ENST00000322776.10:c.926G>A	ENSP00000322450.6:p.Gly309Asp
ENST00000415352.6:c.905G>A	ENSP00000395368.2:p.Gly302Asp
ENST00000526169.1:n.656-107G>A
ENST00000526770.5:n.1209G>A
ENST00000527355.5:c.215G>A	ENSP00000432637.1:p.Gly72Asp
ENST00000527923.1:n.268G>A
ENST00000529927.5:c.899G>A	ENSP00000436766.1:p.Gly300Asp
ENST00000532303.5:c.623G>A	ENSP00000432015.1:p.Gly208Asp
ENST00000533919.5:c.392-62G>A	ENSP00000435199.1:n.392-62G>A
NM_001166102.1:c.899G>A	NP_001159574.1:p.Gly300Asp
NM_007103.3:c.926G>A	NP_009034.2:p.Gly309Asp
NM_001166102.2:c.899G>A	NP_001159574.1:p.Gly300Asp
NM_007103.4:c.926G>A MANE Select	NP_009034.2:p.Gly309Asp