Canonical Allele Identifier: CA1888890015

Gene: ATP5F1C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.7794305G= , CM000672.2:g.7794305G=	GRCh38
NC_000010.10:g.7836268G= , CM000672.1:g.7836268G=	GRCh37
NC_000010.9:g.7876274G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356708.12:c.57-1816G= MANE Select	ENSP00000349142.7:n.57-1816G=
ENST00000335698.4:c.57-1816G=	ENSP00000338568.4:n.57-1816G=
ENST00000356708.11:c.57-1816G=	ENSP00000349142.7:n.57-1816G=
ENST00000460362.5:n.90-1816G=
ENST00000460820.6:n.81-1816G=
ENST00000462760.1:n.106-1816G=
ENST00000465936.5:n.86-1816G=
ENST00000472202.1:n.55-1816G=
ENST00000493053.5:n.118-2742G=
NM_001001973.1:c.57-1816G=	NP_001001973.1:n.57-1816G=
NM_005174.2:c.57-1816G=	NP_005165.1:n.57-1816G=
XM_011519490.1:c.-50-2742G=	XP_011517792.1:n.-50-2742G=
NM_001001973.2:c.57-1816G=	NP_001001973.1:n.57-1816G=
NM_001320886.1:c.-50-2742G=	NP_001307815.1:n.-50-2742G=
NM_005174.3:c.57-1816G=	NP_005165.1:n.57-1816G=
XM_017016290.1:c.-50-2742G=	XP_016871779.1:n.-50-2742G=
NM_001001973.3:c.57-1816G= MANE Select	NP_001001973.1:n.57-1816G=
NM_001320886.2:c.-50-2742G=	NP_001307815.1:n.-50-2742G=
NM_005174.4:c.57-1816G=	NP_005165.1:n.57-1816G=