Canonical Allele Identifier: CA381540784

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378942C>A (hg19) ; chr11:g.67611471C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611471C>A , CM000673.2:g.67611471C>A	GRCh38
NC_000011.9:g.67378942C>A , CM000673.1:g.67378942C>A	GRCh37
NC_000011.8:g.67135518C>A	NCBI36
NG_013353.1:g.9620C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.982C>A MANE Select	ENSP00000322450.6:p.Pro328Thr
ENST00000647561.1:c.982C>A	ENSP00000497587.1:p.Pro328Thr
ENST00000322776.10:c.982C>A	ENSP00000322450.6:p.Pro328Thr
ENST00000415352.6:c.961C>A	ENSP00000395368.2:p.Pro321Thr
ENST00000526169.1:n.656-51C>A
ENST00000526770.5:n.1265C>A
ENST00000527355.5:c.271C>A	ENSP00000432637.1:p.Pro91Thr
ENST00000527923.1:n.324C>A
ENST00000529927.5:c.955C>A	ENSP00000436766.1:p.Pro319Thr
ENST00000532303.5:c.679C>A	ENSP00000432015.1:p.Pro227Thr
ENST00000533919.5:c.392-6C>A	ENSP00000435199.1:n.392-6C>A
NM_001166102.1:c.955C>A	NP_001159574.1:p.Pro319Thr
NM_007103.3:c.982C>A	NP_009034.2:p.Pro328Thr
NM_001166102.2:c.955C>A	NP_001159574.1:p.Pro319Thr
NM_007103.4:c.982C>A MANE Select	NP_009034.2:p.Pro328Thr