Canonical Allele Identifier: CA1444632432
Gene: PPARGC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23814173G= , CM000666.2:g.23814173G= GRCh38
NC_000004.11:g.23815796G= , CM000666.1:g.23815796G= GRCh37
NC_000004.10:g.23424894G= NCBI36
NG_028250.1:g.80905C=
NG_028250.2:g.663803C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264867.7:c.1310C= MANE Select ENSP00000264867.2:p.Thr437=
ENST00000264867.6:c.1310C= ENSP00000264867.2:p.Thr437=
ENST00000506055.5:c.*525C= ENSP00000423075.1:n.*525C=
ENST00000509702.5:n.1350C=
ENST00000613098.4:c.929C= ENSP00000481498.1:p.Thr310=
NM_013261.3:c.1310C= NP_037393.1:p.Thr437=
XM_005248130.2:c.1325C= XP_005248187.1:p.Thr442=
XM_005248131.3:c.1322C= XP_005248188.1:p.Thr441=
XM_005248132.1:c.1301C= XP_005248189.1:p.Thr434=
XM_005248134.3:c.1325C= XP_005248191.1:p.Thr442=
XM_011513764.1:c.1310C= XP_011512066.1:p.Thr437=
XM_011513765.1:c.1274C= XP_011512067.1:p.Thr425=
XM_011513766.1:c.1205C= XP_011512068.1:p.Thr402=
XM_011513767.1:c.1205C= XP_011512069.1:p.Thr402=
XM_011513768.1:c.1205C= XP_011512070.1:p.Thr402=
XM_011513769.1:c.1325C= XP_011512071.1:p.Thr442=
XM_011513770.1:c.929C= XP_011512072.1:p.Thr310=
XM_011513771.1:c.929C= XP_011512073.1:p.Thr310=
NM_001330751.1:c.1325C= NP_001317680.1:p.Thr442=
NM_001330752.1:c.1274C= NP_001317681.1:p.Thr425=
NM_001330753.1:c.929C= NP_001317682.1:p.Thr310=
NM_001354825.1:c.1325C= NP_001341754.1:p.Thr442=
NM_001354826.1:c.929C= NP_001341755.1:p.Thr310=
NM_001354827.1:c.1325C= NP_001341756.1:p.Thr442=
NM_013261.4:c.1310C= NP_037393.1:p.Thr437=
NR_148981.1:n.1837C=
NR_148982.1:n.1910C=
NR_148983.1:n.2063C=
NR_148984.1:n.1461C=
NR_148985.1:n.1975C=
NR_148986.1:n.1980C=
NR_148987.1:n.2062C=
XM_005248131.5:c.1322C= XP_005248188.1:p.Thr441=
XM_005248134.4:c.1325C= XP_005248191.1:p.Thr442=
XM_011513769.2:c.1325C= XP_011512071.1:p.Thr442=
XM_024453878.1:c.1325C= XP_024309646.1:p.Thr442=
NM_013261.5:c.1310C= MANE Select NP_037393.1:p.Thr437=
NM_001330751.2:c.1325C= NP_001317680.1:p.Thr442=
NM_001330752.2:c.1274C= NP_001317681.1:p.Thr425=
NM_001354825.2:c.1325C= NP_001341754.1:p.Thr442=
NM_001354826.2:c.929C= NP_001341755.1:p.Thr310=
NM_001354827.2:c.1325C= NP_001341756.1:p.Thr442=
NR_148981.2:n.1913C=
NR_148982.2:n.1986C=
NR_148983.2:n.2139C=
NR_148984.2:n.1431C=
NR_148985.2:n.2051C=
NR_148986.2:n.2056C=
NR_148987.2:n.2138C=
NM_001330753.2:c.929C= NP_001317682.1:p.Thr310=