Canonical Allele Identifier: CA1444632056
Gene: PPARGC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23814048C= , CM000666.2:g.23814048C= GRCh38
NC_000004.11:g.23815671C= , CM000666.1:g.23815671C= GRCh37
NC_000004.10:g.23424769C= NCBI36
NG_028250.1:g.81030G=
NG_028250.2:g.663928G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264867.7:c.1435G= MANE Select ENSP00000264867.2:p.Asp479=
ENST00000264867.6:c.1435G= ENSP00000264867.2:p.Asp479=
ENST00000506055.5:c.*650G= ENSP00000423075.1:n.*650G=
ENST00000509702.5:n.1475G=
ENST00000613098.4:c.1054G= ENSP00000481498.1:p.Asp352=
NM_013261.3:c.1435G= NP_037393.1:p.Asp479=
XM_005248130.2:c.1450G= XP_005248187.1:p.Asp484=
XM_005248131.3:c.1447G= XP_005248188.1:p.Asp483=
XM_005248132.1:c.1426G= XP_005248189.1:p.Asp476=
XM_005248134.3:c.1450G= XP_005248191.1:p.Asp484=
XM_011513764.1:c.1435G= XP_011512066.1:p.Asp479=
XM_011513765.1:c.1399G= XP_011512067.1:p.Asp467=
XM_011513766.1:c.1330G= XP_011512068.1:p.Asp444=
XM_011513767.1:c.1330G= XP_011512069.1:p.Asp444=
XM_011513768.1:c.1330G= XP_011512070.1:p.Asp444=
XM_011513769.1:c.1450G= XP_011512071.1:p.Asp484=
XM_011513770.1:c.1054G= XP_011512072.1:p.Asp352=
XM_011513771.1:c.1054G= XP_011512073.1:p.Asp352=
NM_001330751.1:c.1450G= NP_001317680.1:p.Asp484=
NM_001330752.1:c.1399G= NP_001317681.1:p.Asp467=
NM_001330753.1:c.1054G= NP_001317682.1:p.Asp352=
NM_001354825.1:c.1450G= NP_001341754.1:p.Asp484=
NM_001354826.1:c.1054G= NP_001341755.1:p.Asp352=
NM_001354827.1:c.1450G= NP_001341756.1:p.Asp484=
NM_013261.4:c.1435G= NP_037393.1:p.Asp479=
NR_148981.1:n.1962G=
NR_148982.1:n.2035G=
NR_148983.1:n.2188G=
NR_148984.1:n.1586G=
NR_148985.1:n.2100G=
NR_148986.1:n.2105G=
NR_148987.1:n.2187G=
XM_005248131.5:c.1447G= XP_005248188.1:p.Asp483=
XM_005248134.4:c.1450G= XP_005248191.1:p.Asp484=
XM_011513769.2:c.1450G= XP_011512071.1:p.Asp484=
XM_024453878.1:c.1450G= XP_024309646.1:p.Asp484=
NM_013261.5:c.1435G= MANE Select NP_037393.1:p.Asp479=
NM_001330751.2:c.1450G= NP_001317680.1:p.Asp484=
NM_001330752.2:c.1399G= NP_001317681.1:p.Asp467=
NM_001354825.2:c.1450G= NP_001341754.1:p.Asp484=
NM_001354826.2:c.1054G= NP_001341755.1:p.Asp352=
NM_001354827.2:c.1450G= NP_001341756.1:p.Asp484=
NR_148981.2:n.2038G=
NR_148982.2:n.2111G=
NR_148983.2:n.2264G=
NR_148984.2:n.1556G=
NR_148985.2:n.2176G=
NR_148986.2:n.2181G=
NR_148987.2:n.2263G=
NM_001330753.2:c.1054G= NP_001317682.1:p.Asp352=