Canonical Allele Identifier: CA1888889790
Gene: ATP5F1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.7794045T= , CM000672.2:g.7794045T= GRCh38
NC_000010.10:g.7836008T= , CM000672.1:g.7836008T= GRCh37
NC_000010.9:g.7876014T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356708.12:c.57-2076T= MANE Select ENSP00000349142.7:n.57-2076T=
ENST00000335698.4:c.57-2076T= ENSP00000338568.4:n.57-2076T=
ENST00000356708.11:c.57-2076T= ENSP00000349142.7:n.57-2076T=
ENST00000460362.5:n.90-2076T=
ENST00000460820.6:n.81-2076T=
ENST00000462760.1:n.106-2076T=
ENST00000465936.5:n.86-2076T=
ENST00000472202.1:n.55-2076T=
ENST00000493053.5:n.118-3002T=
NM_001001973.1:c.57-2076T= NP_001001973.1:n.57-2076T=
NM_005174.2:c.57-2076T= NP_005165.1:n.57-2076T=
XM_011519490.1:c.-50-3002T= XP_011517792.1:n.-50-3002T=
NM_001001973.2:c.57-2076T= NP_001001973.1:n.57-2076T=
NM_001320886.1:c.-50-3002T= NP_001307815.1:n.-50-3002T=
NM_005174.3:c.57-2076T= NP_005165.1:n.57-2076T=
XM_017016290.1:c.-50-3002T= XP_016871779.1:n.-50-3002T=
NM_001001973.3:c.57-2076T= MANE Select NP_001001973.1:n.57-2076T=
NM_001320886.2:c.-50-3002T= NP_001307815.1:n.-50-3002T=
NM_005174.4:c.57-2076T= NP_005165.1:n.57-2076T=