Canonical Allele Identifier: CA11826273
Gene: PPARGC1A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13131226

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23873358C>T , CM000666.2:g.23873358C>T GRCh38
NC_000004.11:g.23874981C>T , CM000666.1:g.23874981C>T GRCh37
NC_000004.10:g.23484079C>T NCBI36
NG_028250.1:g.21720G>A
NG_028250.2:g.604618G>A

Transcript Alleles

HGVS Amino-acid change
NM_013261.3:c.234+11394G>A VV NP_037393.1:p.=
XM_005248130.2:c.249+11394G>A XP_005248187.1:p.=
XM_005248131.3:c.246+11394G>A XP_005248188.1:p.=
XM_005248132.1:c.225+11394G>A XP_005248189.1:p.=
XM_005248134.3:c.249+11394G>A XP_005248191.1:p.=
XM_011513764.1:c.234+11394G>A XP_011512066.1:p.=
XM_011513765.1:c.198+11394G>A XP_011512067.1:p.=
XM_011513766.1:c.129+4356G>A XP_011512068.1:p.=
XM_011513767.1:c.129+4356G>A XP_011512069.1:p.=
XM_011513768.1:c.129+4356G>A XP_011512070.1:p.=
XM_011513769.1:c.249+11394G>A XP_011512071.1:p.=
XM_011513770.1:c.-148+7371G>A XP_011512072.1:p.=
XM_011513771.1:c.-148+8600G>A XP_011512073.1:p.=
NM_001330751.1:c.249+11394G>A VV NP_001317680.1:p.=
NM_001330752.1:c.198+11394G>A VV NP_001317681.1:p.=
NM_001330753.1:c.-148+7371G>A VV NP_001317682.1:p.=
NM_001354825.1:c.249+11394G>A VV NP_001341754.1:p.=
NM_001354826.1:c.-148+10953G>A VV NP_001341755.1:p.=
NM_001354827.1:c.249+11394G>A VV NP_001341756.1:p.=
NM_013261.4:c.234+11394G>A VV
NR_148981.1:n.700+11394G>A
NR_148982.1:n.803+11394G>A
NR_148983.1:n.956+4356G>A
NR_148984.1:n.354+11394G>A
NR_148985.1:n.868+11394G>A
NR_148986.1:n.700+11394G>A
NR_148987.1:n.700+11394G>A
XM_005248131.5:c.246+11394G>A
XM_005248134.4:c.249+11394G>A
XM_011513769.2:c.249+11394G>A
XM_024453878.1:c.249+11394G>A XP_024309646.1:p.=
NM_013261.5:c.234+11394G>A VV MANE Preferred
ENST00000264867.6:c.234+11394G>A ENSP00000264867.2:p.=
ENST00000506055.5:c.234+11394G>A ENSP00000423075.1:p.=
ENST00000507342.5:n.314+11394G>A
ENST00000508380.1:n.154+8600G>A
ENST00000509642.5:n.327+4356G>A
ENST00000509702.5:n.191+8563G>A
ENST00000512169.1:n.327+4356G>A
ENST00000513205.5:c.234+11394G>A ENSP00000421632.1:p.=
ENST00000515534.5:n.307-7112G>A
ENST00000612355.1:c.222+11394G>A ENSP00000479729.1:p.=
ENST00000613098.4:c.-148+7371G>A ENSP00000481498.1:p.=
ENST00000617484.4:c.222+11394G>A ENSP00000477921.1:p.=