Canonical Allele Identifier: CA2786552495

Gene: ATP5F1C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.7794322del , CM000672.2:g.7794322del	GRCh38
NC_000010.10:g.7836285del , CM000672.1:g.7836285del	GRCh37
NC_000010.9:g.7876291del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356708.12:c.57-1799del MANE Select	ENSP00000349142.7:n.57-1799del
ENST00000335698.4:c.57-1799del	ENSP00000338568.4:n.57-1799del
ENST00000356708.11:c.57-1799del	ENSP00000349142.7:n.57-1799del
ENST00000460362.5:n.90-1799del
ENST00000460820.6:n.81-1799del
ENST00000462760.1:n.106-1799del
ENST00000465936.5:n.86-1799del
ENST00000472202.1:n.55-1799del
ENST00000493053.5:n.118-2725del
NM_001001973.1:c.57-1799del	NP_001001973.1:n.57-1799del
NM_005174.2:c.57-1799del	NP_005165.1:n.57-1799del
XM_011519490.1:c.-50-2725del	XP_011517792.1:n.-50-2725del
NM_001001973.2:c.57-1799del	NP_001001973.1:n.57-1799del
NM_001320886.1:c.-50-2725del	NP_001307815.1:n.-50-2725del
NM_005174.3:c.57-1799del	NP_005165.1:n.57-1799del
XM_017016290.1:c.-50-2725del	XP_016871779.1:n.-50-2725del
NM_001001973.3:c.57-1799del MANE Select	NP_001001973.1:n.57-1799del
NM_001320886.2:c.-50-2725del	NP_001307815.1:n.-50-2725del
NM_005174.4:c.57-1799del	NP_005165.1:n.57-1799del