Canonical Allele Identifier: CA356524734

Gene: PPARGC1A

Linked Data

• dbSNP Id: rs1332239268
• gnomAD v2: 4-23815852-A-C
• gnomAD v4: 4-23814229-A-C
• MyVariant Identifiers: chr4:g.23815852A>C (hg19) ; chr4:g.23814229A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814229A>C , CM000666.2:g.23814229A>C	GRCh38
NC_000004.11:g.23815852A>C , CM000666.1:g.23815852A>C	GRCh37
NC_000004.10:g.23424950A>C	NCBI36
NG_028250.1:g.80849T>G
NG_028250.2:g.663747T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1254T>G MANE Select	ENSP00000264867.2:p.Asp418Glu
ENST00000264867.6:c.1254T>G	ENSP00000264867.2:p.Asp418Glu
ENST00000506055.5:c.*469T>G	ENSP00000423075.1:n.*469T>G
ENST00000509702.5:n.1294T>G
ENST00000613098.4:c.873T>G	ENSP00000481498.1:p.Asp291Glu
NM_013261.3:c.1254T>G	NP_037393.1:p.Asp418Glu
XM_005248130.2:c.1269T>G	XP_005248187.1:p.Asp423Glu
XM_005248131.3:c.1266T>G	XP_005248188.1:p.Asp422Glu
XM_005248132.1:c.1245T>G	XP_005248189.1:p.Asp415Glu
XM_005248134.3:c.1269T>G	XP_005248191.1:p.Asp423Glu
XM_011513764.1:c.1254T>G	XP_011512066.1:p.Asp418Glu
XM_011513765.1:c.1218T>G	XP_011512067.1:p.Asp406Glu
XM_011513766.1:c.1149T>G	XP_011512068.1:p.Asp383Glu
XM_011513767.1:c.1149T>G	XP_011512069.1:p.Asp383Glu
XM_011513768.1:c.1149T>G	XP_011512070.1:p.Asp383Glu
XM_011513769.1:c.1269T>G	XP_011512071.1:p.Asp423Glu
XM_011513770.1:c.873T>G	XP_011512072.1:p.Asp291Glu
XM_011513771.1:c.873T>G	XP_011512073.1:p.Asp291Glu
NM_001330751.1:c.1269T>G	NP_001317680.1:p.Asp423Glu
NM_001330752.1:c.1218T>G	NP_001317681.1:p.Asp406Glu
NM_001330753.1:c.873T>G	NP_001317682.1:p.Asp291Glu
NM_001354825.1:c.1269T>G	NP_001341754.1:p.Asp423Glu
NM_001354826.1:c.873T>G	NP_001341755.1:p.Asp291Glu
NM_001354827.1:c.1269T>G	NP_001341756.1:p.Asp423Glu
NM_013261.4:c.1254T>G	NP_037393.1:p.Asp418Glu
NR_148981.1:n.1781T>G
NR_148982.1:n.1854T>G
NR_148983.1:n.2007T>G
NR_148984.1:n.1405T>G
NR_148985.1:n.1919T>G
NR_148986.1:n.1924T>G
NR_148987.1:n.2006T>G
XM_005248131.5:c.1266T>G	XP_005248188.1:p.Asp422Glu
XM_005248134.4:c.1269T>G	XP_005248191.1:p.Asp423Glu
XM_011513769.2:c.1269T>G	XP_011512071.1:p.Asp423Glu
XM_024453878.1:c.1269T>G	XP_024309646.1:p.Asp423Glu
NM_013261.5:c.1254T>G MANE Select	NP_037393.1:p.Asp418Glu
NM_001330751.2:c.1269T>G	NP_001317680.1:p.Asp423Glu
NM_001330752.2:c.1218T>G	NP_001317681.1:p.Asp406Glu
NM_001354825.2:c.1269T>G	NP_001341754.1:p.Asp423Glu
NM_001354826.2:c.873T>G	NP_001341755.1:p.Asp291Glu
NM_001354827.2:c.1269T>G	NP_001341756.1:p.Asp423Glu
NR_148981.2:n.1857T>G
NR_148982.2:n.1930T>G
NR_148983.2:n.2083T>G
NR_148984.2:n.1375T>G
NR_148985.2:n.1995T>G
NR_148986.2:n.2000T>G
NR_148987.2:n.2082T>G
NM_001330753.2:c.873T>G	NP_001317682.1:p.Asp291Glu