Canonical Allele Identifier: CA918903893

Gene: NDUFV1

Linked Data

• dbSNP Id: rs1565226094
• gnomAD v4: 11-67611986-TCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611987_67611988del , CM000673.2:g.67611987_67611988del	GRCh38
NC_000011.9:g.67379458_67379459del , CM000673.1:g.67379458_67379459del	GRCh37
NC_000011.8:g.67136034_67136035del	NCBI36
NG_013353.1:g.10136_10137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1162+9_1162+10del MANE Select	ENSP00000322450.6:n.1162+9_1162+10del
ENST00000647561.1:c.1162+9_1162+10del	ENSP00000497587.1:n.1162+9_1162+10del
ENST00000322776.10:c.1162+9_1162+10del	ENSP00000322450.6:n.1162+9_1162+10del
ENST00000415352.6:c.1141+9_1141+10del	ENSP00000395368.2:n.1141+9_1141+10del
ENST00000526770.5:n.1445+9_1445+10del
ENST00000527355.5:c.370-133_370-132del	ENSP00000432637.1:n.370-133_370-132del
ENST00000527923.1:n.504+9_504+10del
ENST00000529927.5:c.1135+9_1135+10del	ENSP00000436766.1:n.1135+9_1135+10del
ENST00000531250.1:n.426+9_426+10del
ENST00000532303.5:c.859+9_859+10del	ENSP00000432015.1:n.859+9_859+10del
ENST00000533919.5:c.566+9_566+10del	ENSP00000435199.1:n.566+9_566+10del
ENST00000534352.1:n.269_270del
NM_001166102.1:c.1135+9_1135+10del	NP_001159574.1:n.1135+9_1135+10del
NM_007103.3:c.1162+9_1162+10del	NP_009034.2:n.1162+9_1162+10del
NM_001166102.2:c.1135+9_1135+10del	NP_001159574.1:n.1135+9_1135+10del
NM_007103.4:c.1162+9_1162+10del MANE Select	NP_009034.2:n.1162+9_1162+10del