Canonical Allele Identifier: CA591496907

Gene: ATP5F1C

Linked Data

• dbSNP Id: rs1339086265
• gnomAD v2: 10-7836151-G-C
• gnomAD v3: 10-7794188-G-C
• gnomAD v4: 10-7794188-G-C
• MyVariant Identifiers: chr10:g.7836151G>C (hg19) ; chr10:g.7794188G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.7794188G>C , CM000672.2:g.7794188G>C	GRCh38
NC_000010.10:g.7836151G>C , CM000672.1:g.7836151G>C	GRCh37
NC_000010.9:g.7876157G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356708.12:c.57-1933G>C MANE Select	ENSP00000349142.7:n.57-1933G>C
ENST00000335698.4:c.57-1933G>C	ENSP00000338568.4:n.57-1933G>C
ENST00000356708.11:c.57-1933G>C	ENSP00000349142.7:n.57-1933G>C
ENST00000460362.5:n.90-1933G>C
ENST00000460820.6:n.81-1933G>C
ENST00000462760.1:n.106-1933G>C
ENST00000465936.5:n.86-1933G>C
ENST00000472202.1:n.55-1933G>C
ENST00000493053.5:n.118-2859G>C
NM_001001973.1:c.57-1933G>C	NP_001001973.1:n.57-1933G>C
NM_005174.2:c.57-1933G>C	NP_005165.1:n.57-1933G>C
XM_011519490.1:c.-50-2859G>C	XP_011517792.1:n.-50-2859G>C
NM_001001973.2:c.57-1933G>C	NP_001001973.1:n.57-1933G>C
NM_001320886.1:c.-50-2859G>C	NP_001307815.1:n.-50-2859G>C
NM_005174.3:c.57-1933G>C	NP_005165.1:n.57-1933G>C
XM_017016290.1:c.-50-2859G>C	XP_016871779.1:n.-50-2859G>C
NM_001001973.3:c.57-1933G>C MANE Select	NP_001001973.1:n.57-1933G>C
NM_001320886.2:c.-50-2859G>C	NP_001307815.1:n.-50-2859G>C
NM_005174.4:c.57-1933G>C	NP_005165.1:n.57-1933G>C