Canonical Allele Identifier: CA503985087

Gene: ATP5F1A

Linked Data

• MyVariant Identifiers: chr18:g.43667436C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087470C>G , CM000680.2:g.46087470C>G	GRCh38
NC_000018.9:g.43667436C>G , CM000680.1:g.43667436C>G	GRCh37
NC_000018.8:g.41921434C>G	NCBI36
NG_041769.1:g.21764G>C
NG_041769.2:g.26764G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.822G>C MANE Select	ENSP00000381736.5:p.Val274=
ENST00000282050.6:c.822G>C	ENSP00000282050.2:p.Val274=
ENST00000398752.10:c.822G>C	ENSP00000381736.5:p.Val274=
ENST00000586523.1:n.1227G>C
ENST00000586592.5:c.*885G>C	ENSP00000466275.3:n.*885G>C
ENST00000589252.5:c.555G>C	ENSP00000466975.1:p.Val185=
ENST00000590156.5:c.*718G>C	ENSP00000466309.1:n.*718G>C
ENST00000590665.5:c.756G>C	ENSP00000467037.1:p.Val252=
ENST00000592364.5:c.227-406G>C	ENSP00000468618.1:n.227-406G>C
ENST00000593152.6:c.672G>C	ENSP00000465477.2:p.Val224=
NM_001001935.2:c.672G>C	NP_001001935.1:p.Val224=
NM_001001937.1:c.822G>C	NP_001001937.1:p.Val274=
NM_001257334.1:c.756G>C	NP_001244263.1:p.Val252=
NM_001257335.1:c.672G>C	NP_001244264.1:p.Val224=
NM_004046.5:c.822G>C	NP_004037.1:p.Val274=
XM_011526018.1:c.672G>C	XP_011524320.1:p.Val224=
XM_017025789.1:c.822G>C	XP_016881278.1:p.Val274=
NM_004046.6:c.822G>C MANE Select	NP_004037.1:p.Val274=
NM_001001935.3:c.672G>C	NP_001001935.1:p.Val224=
NM_001257334.2:c.756G>C	NP_001244263.1:p.Val252=
NM_001001937.2:c.822G>C	NP_001001937.1:p.Val274=
NM_001257335.2:c.672G>C	NP_001244264.1:p.Val224=