Canonical Allele Identifier: CA2875270

Gene: PPARGC1A

Linked Data

• dbSNP Id: rs369980273
• ExAC: 4:23815760 G / C
• gnomAD v2: 4-23815760-G-C
• gnomAD v3: 4-23814137-G-C
• gnomAD v4: 4-23814137-G-C
• MyVariant Identifiers: chr4:g.23815760G>C (hg19) ; chr4:g.23814137G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814137G>C , CM000666.2:g.23814137G>C	GRCh38
NC_000004.11:g.23815760G>C , CM000666.1:g.23815760G>C	GRCh37
NC_000004.10:g.23424858G>C	NCBI36
NG_028250.1:g.80941C>G
NG_028250.2:g.663839C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1346C>G MANE Select	ENSP00000264867.2:p.Thr449Arg
ENST00000264867.6:c.1346C>G	ENSP00000264867.2:p.Thr449Arg
ENST00000506055.5:c.*561C>G	ENSP00000423075.1:n.*561C>G
ENST00000509702.5:n.1386C>G
ENST00000613098.4:c.965C>G	ENSP00000481498.1:p.Thr322Arg
NM_013261.3:c.1346C>G	NP_037393.1:p.Thr449Arg
XM_005248130.2:c.1361C>G	XP_005248187.1:p.Thr454Arg
XM_005248131.3:c.1358C>G	XP_005248188.1:p.Thr453Arg
XM_005248132.1:c.1337C>G	XP_005248189.1:p.Thr446Arg
XM_005248134.3:c.1361C>G	XP_005248191.1:p.Thr454Arg
XM_011513764.1:c.1346C>G	XP_011512066.1:p.Thr449Arg
XM_011513765.1:c.1310C>G	XP_011512067.1:p.Thr437Arg
XM_011513766.1:c.1241C>G	XP_011512068.1:p.Thr414Arg
XM_011513767.1:c.1241C>G	XP_011512069.1:p.Thr414Arg
XM_011513768.1:c.1241C>G	XP_011512070.1:p.Thr414Arg
XM_011513769.1:c.1361C>G	XP_011512071.1:p.Thr454Arg
XM_011513770.1:c.965C>G	XP_011512072.1:p.Thr322Arg
XM_011513771.1:c.965C>G	XP_011512073.1:p.Thr322Arg
NM_001330751.1:c.1361C>G	NP_001317680.1:p.Thr454Arg
NM_001330752.1:c.1310C>G	NP_001317681.1:p.Thr437Arg
NM_001330753.1:c.965C>G	NP_001317682.1:p.Thr322Arg
NM_001354825.1:c.1361C>G	NP_001341754.1:p.Thr454Arg
NM_001354826.1:c.965C>G	NP_001341755.1:p.Thr322Arg
NM_001354827.1:c.1361C>G	NP_001341756.1:p.Thr454Arg
NM_013261.4:c.1346C>G	NP_037393.1:p.Thr449Arg
NR_148981.1:n.1873C>G
NR_148982.1:n.1946C>G
NR_148983.1:n.2099C>G
NR_148984.1:n.1497C>G
NR_148985.1:n.2011C>G
NR_148986.1:n.2016C>G
NR_148987.1:n.2098C>G
XM_005248131.5:c.1358C>G	XP_005248188.1:p.Thr453Arg
XM_005248134.4:c.1361C>G	XP_005248191.1:p.Thr454Arg
XM_011513769.2:c.1361C>G	XP_011512071.1:p.Thr454Arg
XM_024453878.1:c.1361C>G	XP_024309646.1:p.Thr454Arg
NM_013261.5:c.1346C>G MANE Select	NP_037393.1:p.Thr449Arg
NM_001330751.2:c.1361C>G	NP_001317680.1:p.Thr454Arg
NM_001330752.2:c.1310C>G	NP_001317681.1:p.Thr437Arg
NM_001354825.2:c.1361C>G	NP_001341754.1:p.Thr454Arg
NM_001354826.2:c.965C>G	NP_001341755.1:p.Thr322Arg
NM_001354827.2:c.1361C>G	NP_001341756.1:p.Thr454Arg
NR_148981.2:n.1949C>G
NR_148982.2:n.2022C>G
NR_148983.2:n.2175C>G
NR_148984.2:n.1467C>G
NR_148985.2:n.2087C>G
NR_148986.2:n.2092C>G
NR_148987.2:n.2174C>G
NM_001330753.2:c.965C>G	NP_001317682.1:p.Thr322Arg