Canonical Allele Identifier: CA668621864

Gene: ATP5F1C

Linked Data

• dbSNP Id: rs1437009232
• gnomAD v3: 10-7793950-AGT-A
• gnomAD v4: 10-7793950-AGT-A
• MyVariant Identifiers: chr10:g.7835914_7835915del (hg19) ; chr10:g.7793951_7793952del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.7793953_7793954del , CM000672.2:g.7793953_7793954del	GRCh38
NC_000010.10:g.7835916_7835917del , CM000672.1:g.7835916_7835917del	GRCh37
NC_000010.9:g.7875922_7875923del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356708.12:c.57-2168_57-2167del MANE Select	ENSP00000349142.7:n.57-2168_57-2167del
ENST00000335698.4:c.57-2168_57-2167del	ENSP00000338568.4:n.57-2168_57-2167del
ENST00000356708.11:c.57-2168_57-2167del	ENSP00000349142.7:n.57-2168_57-2167del
ENST00000460362.5:n.90-2168_90-2167del
ENST00000460820.6:n.81-2168_81-2167del
ENST00000462760.1:n.106-2168_106-2167del
ENST00000465936.5:n.86-2168_86-2167del
ENST00000472202.1:n.55-2168_55-2167del
ENST00000493053.5:n.118-3094_118-3093del
NM_001001973.1:c.57-2168_57-2167del	NP_001001973.1:n.57-2168_57-2167del
NM_005174.2:c.57-2168_57-2167del	NP_005165.1:n.57-2168_57-2167del
XM_011519490.1:c.-50-3094_-50-3093del	XP_011517792.1:n.-50-3094_-50-3093del
NM_001001973.2:c.57-2168_57-2167del	NP_001001973.1:n.57-2168_57-2167del
NM_001320886.1:c.-50-3094_-50-3093del	NP_001307815.1:n.-50-3094_-50-3093del
NM_005174.3:c.57-2168_57-2167del	NP_005165.1:n.57-2168_57-2167del
XM_017016290.1:c.-50-3094_-50-3093del	XP_016871779.1:n.-50-3094_-50-3093del
NM_001001973.3:c.57-2168_57-2167del MANE Select	NP_001001973.1:n.57-2168_57-2167del
NM_001320886.2:c.-50-3094_-50-3093del	NP_001307815.1:n.-50-3094_-50-3093del
NM_005174.4:c.57-2168_57-2167del	NP_005165.1:n.57-2168_57-2167del