Canonical Allele Identifier: CA793185333

Gene: PPARGC1A

Linked Data

• dbSNP Id: rs11724368
• gnomAD v3: 4-23861310-A-C
• gnomAD v4: 4-23861310-A-C
• MyVariant Identifiers: chr4:g.23862933A>C (hg19) ; chr4:g.23861310A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23861310A>C , CM000666.2:g.23861310A>C	GRCh38
NC_000004.11:g.23862933A>C , CM000666.1:g.23862933A>C	GRCh37
NC_000004.10:g.23472031A>C	NCBI36
NG_028250.1:g.33768T>G
NG_028250.2:g.616666T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264867.7:c.234+23442T>G MANE Select	ENSP00000264867.2:n.234+23442T>G
ENST00000264867.6:c.234+23442T>G	ENSP00000264867.2:n.234+23442T>G
ENST00000506055.5:c.234+23442T>G	ENSP00000423075.1:n.234+23442T>G
ENST00000507342.5:n.314+23442T>G
ENST00000508380.1:n.154+20648T>G
ENST00000509642.5:n.327+16404T>G
ENST00000509702.5:n.191+20611T>G
ENST00000512169.1:n.327+16404T>G
ENST00000513205.5:c.234+23442T>G	ENSP00000421632.1:n.234+23442T>G
ENST00000612355.1:c.222+23442T>G	ENSP00000479729.1:n.222+23442T>G
ENST00000613098.4:c.-148+19419T>G	ENSP00000481498.1:n.-148+19419T>G
ENST00000617484.4:c.222+23442T>G	ENSP00000477921.1:n.222+23442T>G
NM_013261.3:c.234+23442T>G	NP_037393.1:n.234+23442T>G
XM_005248130.2:c.249+23442T>G	XP_005248187.1:n.249+23442T>G
XM_005248131.3:c.246+23442T>G	XP_005248188.1:n.246+23442T>G
XM_005248132.1:c.225+23442T>G	XP_005248189.1:n.225+23442T>G
XM_005248134.3:c.249+23442T>G	XP_005248191.1:n.249+23442T>G
XM_011513764.1:c.234+23442T>G	XP_011512066.1:n.234+23442T>G
XM_011513765.1:c.198+23442T>G	XP_011512067.1:n.198+23442T>G
XM_011513766.1:c.129+16404T>G	XP_011512068.1:n.129+16404T>G
XM_011513767.1:c.129+16404T>G	XP_011512069.1:n.129+16404T>G
XM_011513768.1:c.129+16404T>G	XP_011512070.1:n.129+16404T>G
XM_011513769.1:c.249+23442T>G	XP_011512071.1:n.249+23442T>G
XM_011513770.1:c.-148+19419T>G	XP_011512072.1:n.-148+19419T>G
XM_011513771.1:c.-148+20648T>G	XP_011512073.1:n.-148+20648T>G
NM_001330751.1:c.249+23442T>G	NP_001317680.1:n.249+23442T>G
NM_001330752.1:c.198+23442T>G	NP_001317681.1:n.198+23442T>G
NM_001330753.1:c.-148+19419T>G	NP_001317682.1:n.-148+19419T>G
NM_001354825.1:c.249+23442T>G	NP_001341754.1:n.249+23442T>G
NM_001354826.1:c.-148+23001T>G	NP_001341755.1:n.-148+23001T>G
NM_001354827.1:c.249+23442T>G	NP_001341756.1:n.249+23442T>G
NM_013261.4:c.234+23442T>G	NP_037393.1:n.234+23442T>G
NR_148981.1:n.700+23442T>G
NR_148982.1:n.803+23442T>G
NR_148983.1:n.956+16404T>G
NR_148984.1:n.354+23442T>G
NR_148985.1:n.868+23442T>G
NR_148986.1:n.700+23442T>G
NR_148987.1:n.700+23442T>G
XM_005248131.5:c.246+23442T>G	XP_005248188.1:n.246+23442T>G
XM_005248134.4:c.249+23442T>G	XP_005248191.1:n.249+23442T>G
XM_011513769.2:c.249+23442T>G	XP_011512071.1:n.249+23442T>G
XM_024453878.1:c.249+23442T>G	XP_024309646.1:n.249+23442T>G
NM_013261.5:c.234+23442T>G MANE Select	NP_037393.1:n.234+23442T>G
NM_001330751.2:c.249+23442T>G	NP_001317680.1:n.249+23442T>G
NM_001330752.2:c.198+23442T>G	NP_001317681.1:n.198+23442T>G
NM_001354825.2:c.249+23442T>G	NP_001341754.1:n.249+23442T>G
NM_001354826.2:c.-148+23001T>G	NP_001341755.1:n.-148+23001T>G
NM_001354827.2:c.249+23442T>G	NP_001341756.1:n.249+23442T>G
NR_148981.2:n.776+23442T>G
NR_148982.2:n.879+23442T>G
NR_148983.2:n.1032+16404T>G
NR_148984.2:n.324+23442T>G
NR_148985.2:n.944+23442T>G
NR_148986.2:n.776+23442T>G
NR_148987.2:n.776+23442T>G
NM_001330753.2:c.-148+19419T>G	NP_001317682.1:n.-148+19419T>G