Canonical Allele Identifier: CA1980192913

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611986_67611988delinsTCG , CM000673.2:g.67611986_67611988delinsTCG	GRCh38
NC_000011.9:g.67379457_67379459delinsTCG , CM000673.1:g.67379457_67379459delinsTCG	GRCh37
NC_000011.8:g.67136033_67136035delinsTCG	NCBI36
NG_013353.1:g.10135_10137delinsTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1162+8_1162+10delinsTCG MANE Select	ENSP00000322450.6:n.1162+8_1162+10delinsTCG
ENST00000647561.1:c.1162+8_1162+10delinsTCG	ENSP00000497587.1:n.1162+8_1162+10delinsTCG
ENST00000322776.10:c.1162+8_1162+10delinsTCG	ENSP00000322450.6:n.1162+8_1162+10delinsTCG
ENST00000415352.6:c.1141+8_1141+10delinsTCG	ENSP00000395368.2:n.1141+8_1141+10delinsTCG
ENST00000526770.5:n.1445+8_1445+10delinsTCG
ENST00000527355.5:c.370-134_370-132delinsTCG	ENSP00000432637.1:n.370-134_370-132delinsTCG
ENST00000527923.1:n.504+8_504+10delinsTCG
ENST00000529927.5:c.1135+8_1135+10delinsTCG	ENSP00000436766.1:n.1135+8_1135+10delinsTCG
ENST00000531250.1:n.426+8_426+10delinsTCG
ENST00000532303.5:c.859+8_859+10delinsTCG	ENSP00000432015.1:n.859+8_859+10delinsTCG
ENST00000533919.5:c.566+8_566+10delinsTCG	ENSP00000435199.1:n.566+8_566+10delinsTCG
ENST00000534352.1:n.268_270delinsTCG
NM_001166102.1:c.1135+8_1135+10delinsTCG	NP_001159574.1:n.1135+8_1135+10delinsTCG
NM_007103.3:c.1162+8_1162+10delinsTCG	NP_009034.2:n.1162+8_1162+10delinsTCG
NM_001166102.2:c.1135+8_1135+10delinsTCG	NP_001159574.1:n.1135+8_1135+10delinsTCG
NM_007103.4:c.1162+8_1162+10delinsTCG MANE Select	NP_009034.2:n.1162+8_1162+10delinsTCG