Canonical Allele Identifier: CA1444632132
Gene: PPARGC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23814109G= , CM000666.2:g.23814109G= GRCh38
NC_000004.11:g.23815732G= , CM000666.1:g.23815732G= GRCh37
NC_000004.10:g.23424830G= NCBI36
NG_028250.1:g.80969C=
NG_028250.2:g.663867C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264867.7:c.1374C= MANE Select ENSP00000264867.2:p.Ile458=
ENST00000264867.6:c.1374C= ENSP00000264867.2:p.Ile458=
ENST00000506055.5:c.*589C= ENSP00000423075.1:n.*589C=
ENST00000509702.5:n.1414C=
ENST00000613098.4:c.993C= ENSP00000481498.1:p.Ile331=
NM_013261.3:c.1374C= NP_037393.1:p.Ile458=
XM_005248130.2:c.1389C= XP_005248187.1:p.Ile463=
XM_005248131.3:c.1386C= XP_005248188.1:p.Ile462=
XM_005248132.1:c.1365C= XP_005248189.1:p.Ile455=
XM_005248134.3:c.1389C= XP_005248191.1:p.Ile463=
XM_011513764.1:c.1374C= XP_011512066.1:p.Ile458=
XM_011513765.1:c.1338C= XP_011512067.1:p.Ile446=
XM_011513766.1:c.1269C= XP_011512068.1:p.Ile423=
XM_011513767.1:c.1269C= XP_011512069.1:p.Ile423=
XM_011513768.1:c.1269C= XP_011512070.1:p.Ile423=
XM_011513769.1:c.1389C= XP_011512071.1:p.Ile463=
XM_011513770.1:c.993C= XP_011512072.1:p.Ile331=
XM_011513771.1:c.993C= XP_011512073.1:p.Ile331=
NM_001330751.1:c.1389C= NP_001317680.1:p.Ile463=
NM_001330752.1:c.1338C= NP_001317681.1:p.Ile446=
NM_001330753.1:c.993C= NP_001317682.1:p.Ile331=
NM_001354825.1:c.1389C= NP_001341754.1:p.Ile463=
NM_001354826.1:c.993C= NP_001341755.1:p.Ile331=
NM_001354827.1:c.1389C= NP_001341756.1:p.Ile463=
NM_013261.4:c.1374C= NP_037393.1:p.Ile458=
NR_148981.1:n.1901C=
NR_148982.1:n.1974C=
NR_148983.1:n.2127C=
NR_148984.1:n.1525C=
NR_148985.1:n.2039C=
NR_148986.1:n.2044C=
NR_148987.1:n.2126C=
XM_005248131.5:c.1386C= XP_005248188.1:p.Ile462=
XM_005248134.4:c.1389C= XP_005248191.1:p.Ile463=
XM_011513769.2:c.1389C= XP_011512071.1:p.Ile463=
XM_024453878.1:c.1389C= XP_024309646.1:p.Ile463=
NM_013261.5:c.1374C= MANE Select NP_037393.1:p.Ile458=
NM_001330751.2:c.1389C= NP_001317680.1:p.Ile463=
NM_001330752.2:c.1338C= NP_001317681.1:p.Ile446=
NM_001354825.2:c.1389C= NP_001341754.1:p.Ile463=
NM_001354826.2:c.993C= NP_001341755.1:p.Ile331=
NM_001354827.2:c.1389C= NP_001341756.1:p.Ile463=
NR_148981.2:n.1977C=
NR_148982.2:n.2050C=
NR_148983.2:n.2203C=
NR_148984.2:n.1495C=
NR_148985.2:n.2115C=
NR_148986.2:n.2120C=
NR_148987.2:n.2202C=
NM_001330753.2:c.993C= NP_001317682.1:p.Ile331=