Canonical Allele Identifier: CA1444632534
Gene: PPARGC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23814258G= , CM000666.2:g.23814258G= GRCh38
NC_000004.11:g.23815881G= , CM000666.1:g.23815881G= GRCh37
NC_000004.10:g.23424979G= NCBI36
NG_028250.1:g.80820C=
NG_028250.2:g.663718C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264867.7:c.1225C= MANE Select ENSP00000264867.2:p.Gln409=
ENST00000264867.6:c.1225C= ENSP00000264867.2:p.Gln409=
ENST00000506055.5:c.*440C= ENSP00000423075.1:n.*440C=
ENST00000509702.5:n.1265C=
ENST00000613098.4:c.844C= ENSP00000481498.1:p.Gln282=
NM_013261.3:c.1225C= NP_037393.1:p.Gln409=
XM_005248130.2:c.1240C= XP_005248187.1:p.Gln414=
XM_005248131.3:c.1237C= XP_005248188.1:p.Gln413=
XM_005248132.1:c.1216C= XP_005248189.1:p.Gln406=
XM_005248134.3:c.1240C= XP_005248191.1:p.Gln414=
XM_011513764.1:c.1225C= XP_011512066.1:p.Gln409=
XM_011513765.1:c.1189C= XP_011512067.1:p.Gln397=
XM_011513766.1:c.1120C= XP_011512068.1:p.Gln374=
XM_011513767.1:c.1120C= XP_011512069.1:p.Gln374=
XM_011513768.1:c.1120C= XP_011512070.1:p.Gln374=
XM_011513769.1:c.1240C= XP_011512071.1:p.Gln414=
XM_011513770.1:c.844C= XP_011512072.1:p.Gln282=
XM_011513771.1:c.844C= XP_011512073.1:p.Gln282=
NM_001330751.1:c.1240C= NP_001317680.1:p.Gln414=
NM_001330752.1:c.1189C= NP_001317681.1:p.Gln397=
NM_001330753.1:c.844C= NP_001317682.1:p.Gln282=
NM_001354825.1:c.1240C= NP_001341754.1:p.Gln414=
NM_001354826.1:c.844C= NP_001341755.1:p.Gln282=
NM_001354827.1:c.1240C= NP_001341756.1:p.Gln414=
NM_013261.4:c.1225C= NP_037393.1:p.Gln409=
NR_148981.1:n.1752C=
NR_148982.1:n.1825C=
NR_148983.1:n.1978C=
NR_148984.1:n.1376C=
NR_148985.1:n.1890C=
NR_148986.1:n.1895C=
NR_148987.1:n.1977C=
XM_005248131.5:c.1237C= XP_005248188.1:p.Gln413=
XM_005248134.4:c.1240C= XP_005248191.1:p.Gln414=
XM_011513769.2:c.1240C= XP_011512071.1:p.Gln414=
XM_024453878.1:c.1240C= XP_024309646.1:p.Gln414=
NM_013261.5:c.1225C= MANE Select NP_037393.1:p.Gln409=
NM_001330751.2:c.1240C= NP_001317680.1:p.Gln414=
NM_001330752.2:c.1189C= NP_001317681.1:p.Gln397=
NM_001354825.2:c.1240C= NP_001341754.1:p.Gln414=
NM_001354826.2:c.844C= NP_001341755.1:p.Gln282=
NM_001354827.2:c.1240C= NP_001341756.1:p.Gln414=
NR_148981.2:n.1828C=
NR_148982.2:n.1901C=
NR_148983.2:n.2054C=
NR_148984.2:n.1346C=
NR_148985.2:n.1966C=
NR_148986.2:n.1971C=
NR_148987.2:n.2053C=
NM_001330753.2:c.844C= NP_001317682.1:p.Gln282=