Canonical Allele Identifier: CA402355195

Gene: ATP5F1A

Linked Data

• dbSNP Id: rs1418985544
• gnomAD v2: 18-43667342-G-A
• gnomAD v3: 18-46087376-G-A
• gnomAD v4: 18-46087376-G-A
• MyVariant Identifiers: chr18:g.43667342G>A (hg19) ; chr18:g.46087376G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087376G>A , CM000680.2:g.46087376G>A	GRCh38
NC_000018.9:g.43667342G>A , CM000680.1:g.43667342G>A	GRCh37
NC_000018.8:g.41921340G>A	NCBI36
NG_041769.1:g.21858C>T
NG_041769.2:g.26858C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.916C>T MANE Select	ENSP00000381736.5:p.His306Tyr
ENST00000282050.6:c.916C>T	ENSP00000282050.2:p.His306Tyr
ENST00000398752.10:c.916C>T	ENSP00000381736.5:p.His306Tyr
ENST00000586523.1:n.1321C>T
ENST00000586592.5:c.*979C>T	ENSP00000466275.3:n.*979C>T
ENST00000590156.5:c.*812C>T	ENSP00000466309.1:n.*812C>T
ENST00000590665.5:c.850C>T	ENSP00000467037.1:p.His284Tyr
ENST00000592364.5:c.227-312C>T	ENSP00000468618.1:n.227-312C>T
ENST00000593152.6:c.766C>T	ENSP00000465477.2:p.His256Tyr
NM_001001935.2:c.766C>T	NP_001001935.1:p.His256Tyr
NM_001001937.1:c.916C>T	NP_001001937.1:p.His306Tyr
NM_001257334.1:c.850C>T	NP_001244263.1:p.His284Tyr
NM_001257335.1:c.766C>T	NP_001244264.1:p.His256Tyr
NM_004046.5:c.916C>T	NP_004037.1:p.His306Tyr
XM_011526018.1:c.766C>T	XP_011524320.1:p.His256Tyr
XM_017025789.1:c.916C>T	XP_016881278.1:p.His306Tyr
NM_004046.6:c.916C>T MANE Select	NP_004037.1:p.His306Tyr
NM_001001935.3:c.766C>T	NP_001001935.1:p.His256Tyr
NM_001257334.2:c.850C>T	NP_001244263.1:p.His284Tyr
NM_001001937.2:c.916C>T	NP_001001937.1:p.His306Tyr
NM_001257335.2:c.766C>T	NP_001244264.1:p.His256Tyr