Canonical Allele Identifier: CA924655015

Gene: ATP5F1C

Linked Data

• dbSNP Id: rs1836203706
• gnomAD v3: 10-7794263-GGGCTATTTTTATTCTTT-G
• gnomAD v4: 10-7794263-GGGCTATTTTTATTCTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.7794266_7794282del , CM000672.2:g.7794266_7794282del	GRCh38
NC_000010.10:g.7836229_7836245del , CM000672.1:g.7836229_7836245del	GRCh37
NC_000010.9:g.7876235_7876251del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356708.12:c.57-1855_57-1839del MANE Select	ENSP00000349142.7:n.57-1855_57-1839del
ENST00000335698.4:c.57-1855_57-1839del	ENSP00000338568.4:n.57-1855_57-1839del
ENST00000356708.11:c.57-1855_57-1839del	ENSP00000349142.7:n.57-1855_57-1839del
ENST00000460362.5:n.90-1855_90-1839del
ENST00000460820.6:n.81-1855_81-1839del
ENST00000462760.1:n.106-1855_106-1839del
ENST00000465936.5:n.86-1855_86-1839del
ENST00000472202.1:n.55-1855_55-1839del
ENST00000493053.5:n.118-2781_118-2765del
NM_001001973.1:c.57-1855_57-1839del	NP_001001973.1:n.57-1855_57-1839del
NM_005174.2:c.57-1855_57-1839del	NP_005165.1:n.57-1855_57-1839del
XM_011519490.1:c.-50-2781_-50-2765del	XP_011517792.1:n.-50-2781_-50-2765del
NM_001001973.2:c.57-1855_57-1839del	NP_001001973.1:n.57-1855_57-1839del
NM_001320886.1:c.-50-2781_-50-2765del	NP_001307815.1:n.-50-2781_-50-2765del
NM_005174.3:c.57-1855_57-1839del	NP_005165.1:n.57-1855_57-1839del
XM_017016290.1:c.-50-2781_-50-2765del	XP_016871779.1:n.-50-2781_-50-2765del
NM_001001973.3:c.57-1855_57-1839del MANE Select	NP_001001973.1:n.57-1855_57-1839del
NM_001320886.2:c.-50-2781_-50-2765del	NP_001307815.1:n.-50-2781_-50-2765del
NM_005174.4:c.57-1855_57-1839del	NP_005165.1:n.57-1855_57-1839del