Canonical Allele Identifier: CA402354412

Gene: ATP5F1A

Linked Data

• MyVariant Identifiers: chr18:g.43666972A>C (hg19) ; chr18:g.46087006A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087006A>C , CM000680.2:g.46087006A>C	GRCh38
NC_000018.9:g.43666972A>C , CM000680.1:g.43666972A>C	GRCh37
NC_000018.8:g.41920970A>C	NCBI36
NG_041769.1:g.22228T>G
NG_041769.2:g.27228T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.1176+2T>G MANE Select	ENSP00000381736.5:n.1176+2T>G
ENST00000282050.6:c.1176+2T>G	ENSP00000282050.2:n.1176+2T>G
ENST00000398752.10:c.1176+2T>G	ENSP00000381736.5:n.1176+2T>G
ENST00000586523.1:n.1691T>G
ENST00000586592.5:c.*1239+2T>G	ENSP00000466275.3:n.*1239+2T>G
ENST00000590156.5:c.*1072+2T>G	ENSP00000466309.1:n.*1072+2T>G
ENST00000590665.5:c.1110+2T>G	ENSP00000467037.1:n.1110+2T>G
ENST00000592364.5:c.*49+2T>G	ENSP00000468618.1:n.*49+2T>G
ENST00000593152.6:c.1026+2T>G	ENSP00000465477.2:n.1026+2T>G
NM_001001935.2:c.1026+2T>G	NP_001001935.1:n.1026+2T>G
NM_001001937.1:c.1176+2T>G	NP_001001937.1:n.1176+2T>G
NM_001257334.1:c.1110+2T>G	NP_001244263.1:n.1110+2T>G
NM_001257335.1:c.1026+2T>G	NP_001244264.1:n.1026+2T>G
NM_004046.5:c.1176+2T>G	NP_004037.1:n.1176+2T>G
XM_011526018.1:c.1026+2T>G	XP_011524320.1:n.1026+2T>G
XM_017025789.1:c.1176+2T>G	XP_016881278.1:n.1176+2T>G
NM_004046.6:c.1176+2T>G MANE Select	NP_004037.1:n.1176+2T>G
NM_001001935.3:c.1026+2T>G	NP_001001935.1:n.1026+2T>G
NM_001257334.2:c.1110+2T>G	NP_001244263.1:n.1110+2T>G
NM_001001937.2:c.1176+2T>G	NP_001001937.1:n.1176+2T>G
NM_001257335.2:c.1026+2T>G	NP_001244264.1:n.1026+2T>G