Canonical Allele Identifier: CA1444639883

Gene: PPARGC1A

Linked Data

• dbSNP Id: rs1427003023

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23873209_23873210insAAAGA , CM000666.2:g.23873209_23873210insAAAGA	GRCh38
NC_000004.11:g.23874832_23874833insAAAGA , CM000666.1:g.23874832_23874833insAAAGA	GRCh37
NC_000004.10:g.23483930_23483931insAAAGA	NCBI36
NG_028250.1:g.21869_21870insCTTTT
NG_028250.2:g.604767_604768insCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.234+11543_234+11544insCTTTT MANE Select	ENSP00000264867.2:n.234+11543_234+11544insCTTTT
ENST00000264867.6:c.234+11543_234+11544insCTTTT	ENSP00000264867.2:n.234+11543_234+11544insCTTTT
ENST00000506055.5:c.234+11543_234+11544insCTTTT	ENSP00000423075.1:n.234+11543_234+11544insCTTTT
ENST00000507342.5:n.314+11543_314+11544insCTTTT
ENST00000508380.1:n.154+8749_154+8750insCTTTT
ENST00000509642.5:n.327+4505_327+4506insCTTTT
ENST00000509702.5:n.191+8712_191+8713insCTTTT
ENST00000512169.1:n.327+4505_327+4506insCTTTT
ENST00000513205.5:c.234+11543_234+11544insCTTTT	ENSP00000421632.1:n.234+11543_234+11544insCTTTT
ENST00000515534.5:n.307-6963_307-6962insCTTTT
ENST00000612355.1:c.222+11543_222+11544insCTTTT	ENSP00000479729.1:n.222+11543_222+11544insCTTTT
ENST00000613098.4:c.-148+7520_-148+7521insCTTTT	ENSP00000481498.1:n.-148+7520_-148+7521insCTTTT
ENST00000617484.4:c.222+11543_222+11544insCTTTT	ENSP00000477921.1:n.222+11543_222+11544insCTTTT
NM_013261.3:c.234+11543_234+11544insCTTTT	NP_037393.1:n.234+11543_234+11544insCTTTT
XM_005248130.2:c.249+11543_249+11544insCTTTT	XP_005248187.1:n.249+11543_249+11544insCTTTT
XM_005248131.3:c.246+11543_246+11544insCTTTT	XP_005248188.1:n.246+11543_246+11544insCTTTT
XM_005248132.1:c.225+11543_225+11544insCTTTT	XP_005248189.1:n.225+11543_225+11544insCTTTT
XM_005248134.3:c.249+11543_249+11544insCTTTT	XP_005248191.1:n.249+11543_249+11544insCTTTT
XM_011513764.1:c.234+11543_234+11544insCTTTT	XP_011512066.1:n.234+11543_234+11544insCTTTT
XM_011513765.1:c.198+11543_198+11544insCTTTT	XP_011512067.1:n.198+11543_198+11544insCTTTT
XM_011513766.1:c.129+4505_129+4506insCTTTT	XP_011512068.1:n.129+4505_129+4506insCTTTT
XM_011513767.1:c.129+4505_129+4506insCTTTT	XP_011512069.1:n.129+4505_129+4506insCTTTT
XM_011513768.1:c.129+4505_129+4506insCTTTT	XP_011512070.1:n.129+4505_129+4506insCTTTT
XM_011513769.1:c.249+11543_249+11544insCTTTT	XP_011512071.1:n.249+11543_249+11544insCTTTT
XM_011513770.1:c.-148+7520_-148+7521insCTTTT	XP_011512072.1:n.-148+7520_-148+7521insCTTTT
XM_011513771.1:c.-148+8749_-148+8750insCTTTT	XP_011512073.1:n.-148+8749_-148+8750insCTTTT
NM_001330751.1:c.249+11543_249+11544insCTTTT	NP_001317680.1:n.249+11543_249+11544insCTTTT
NM_001330752.1:c.198+11543_198+11544insCTTTT	NP_001317681.1:n.198+11543_198+11544insCTTTT
NM_001330753.1:c.-148+7520_-148+7521insCTTTT	NP_001317682.1:n.-148+7520_-148+7521insCTTTT
NM_001354825.1:c.249+11543_249+11544insCTTTT	NP_001341754.1:n.249+11543_249+11544insCTTTT
NM_001354826.1:c.-148+11102_-148+11103insCTTTT	NP_001341755.1:n.-148+11102_-148+11103insCTTTT
NM_001354827.1:c.249+11543_249+11544insCTTTT	NP_001341756.1:n.249+11543_249+11544insCTTTT
NM_013261.4:c.234+11543_234+11544insCTTTT	NP_037393.1:n.234+11543_234+11544insCTTTT
NR_148981.1:n.700+11543_700+11544insCTTTT
NR_148982.1:n.803+11543_803+11544insCTTTT
NR_148983.1:n.956+4505_956+4506insCTTTT
NR_148984.1:n.354+11543_354+11544insCTTTT
NR_148985.1:n.868+11543_868+11544insCTTTT
NR_148986.1:n.700+11543_700+11544insCTTTT
NR_148987.1:n.700+11543_700+11544insCTTTT
XM_005248131.5:c.246+11543_246+11544insCTTTT	XP_005248188.1:n.246+11543_246+11544insCTTTT
XM_005248134.4:c.249+11543_249+11544insCTTTT	XP_005248191.1:n.249+11543_249+11544insCTTTT
XM_011513769.2:c.249+11543_249+11544insCTTTT	XP_011512071.1:n.249+11543_249+11544insCTTTT
XM_024453878.1:c.249+11543_249+11544insCTTTT	XP_024309646.1:n.249+11543_249+11544insCTTTT
NM_013261.5:c.234+11543_234+11544insCTTTT MANE Select	NP_037393.1:n.234+11543_234+11544insCTTTT
NM_001330751.2:c.249+11543_249+11544insCTTTT	NP_001317680.1:n.249+11543_249+11544insCTTTT
NM_001330752.2:c.198+11543_198+11544insCTTTT	NP_001317681.1:n.198+11543_198+11544insCTTTT
NM_001354825.2:c.249+11543_249+11544insCTTTT	NP_001341754.1:n.249+11543_249+11544insCTTTT
NM_001354826.2:c.-148+11102_-148+11103insCTTTT	NP_001341755.1:n.-148+11102_-148+11103insCTTTT
NM_001354827.2:c.249+11543_249+11544insCTTTT	NP_001341756.1:n.249+11543_249+11544insCTTTT
NR_148981.2:n.776+11543_776+11544insCTTTT
NR_148982.2:n.879+11543_879+11544insCTTTT
NR_148983.2:n.1032+4505_1032+4506insCTTTT
NR_148984.2:n.324+11543_324+11544insCTTTT
NR_148985.2:n.944+11543_944+11544insCTTTT
NR_148986.2:n.776+11543_776+11544insCTTTT
NR_148987.2:n.776+11543_776+11544insCTTTT
NM_001330753.2:c.-148+7520_-148+7521insCTTTT	NP_001317682.1:n.-148+7520_-148+7521insCTTTT