Canonical Allele Identifier: CA356524656

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815830A>T (hg19) ; chr4:g.23814207A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814207A>T , CM000666.2:g.23814207A>T	GRCh38
NC_000004.11:g.23815830A>T , CM000666.1:g.23815830A>T	GRCh37
NC_000004.10:g.23424928A>T	NCBI36
NG_028250.1:g.80871T>A
NG_028250.2:g.663769T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1276T>A MANE Select	ENSP00000264867.2:p.Ser426Thr
ENST00000264867.6:c.1276T>A	ENSP00000264867.2:p.Ser426Thr
ENST00000506055.5:c.*491T>A	ENSP00000423075.1:n.*491T>A
ENST00000509702.5:n.1316T>A
ENST00000613098.4:c.895T>A	ENSP00000481498.1:p.Ser299Thr
NM_013261.3:c.1276T>A	NP_037393.1:p.Ser426Thr
XM_005248130.2:c.1291T>A	XP_005248187.1:p.Ser431Thr
XM_005248131.3:c.1288T>A	XP_005248188.1:p.Ser430Thr
XM_005248132.1:c.1267T>A	XP_005248189.1:p.Ser423Thr
XM_005248134.3:c.1291T>A	XP_005248191.1:p.Ser431Thr
XM_011513764.1:c.1276T>A	XP_011512066.1:p.Ser426Thr
XM_011513765.1:c.1240T>A	XP_011512067.1:p.Ser414Thr
XM_011513766.1:c.1171T>A	XP_011512068.1:p.Ser391Thr
XM_011513767.1:c.1171T>A	XP_011512069.1:p.Ser391Thr
XM_011513768.1:c.1171T>A	XP_011512070.1:p.Ser391Thr
XM_011513769.1:c.1291T>A	XP_011512071.1:p.Ser431Thr
XM_011513770.1:c.895T>A	XP_011512072.1:p.Ser299Thr
XM_011513771.1:c.895T>A	XP_011512073.1:p.Ser299Thr
NM_001330751.1:c.1291T>A	NP_001317680.1:p.Ser431Thr
NM_001330752.1:c.1240T>A	NP_001317681.1:p.Ser414Thr
NM_001330753.1:c.895T>A	NP_001317682.1:p.Ser299Thr
NM_001354825.1:c.1291T>A	NP_001341754.1:p.Ser431Thr
NM_001354826.1:c.895T>A	NP_001341755.1:p.Ser299Thr
NM_001354827.1:c.1291T>A	NP_001341756.1:p.Ser431Thr
NM_013261.4:c.1276T>A	NP_037393.1:p.Ser426Thr
NR_148981.1:n.1803T>A
NR_148982.1:n.1876T>A
NR_148983.1:n.2029T>A
NR_148984.1:n.1427T>A
NR_148985.1:n.1941T>A
NR_148986.1:n.1946T>A
NR_148987.1:n.2028T>A
XM_005248131.5:c.1288T>A	XP_005248188.1:p.Ser430Thr
XM_005248134.4:c.1291T>A	XP_005248191.1:p.Ser431Thr
XM_011513769.2:c.1291T>A	XP_011512071.1:p.Ser431Thr
XM_024453878.1:c.1291T>A	XP_024309646.1:p.Ser431Thr
NM_013261.5:c.1276T>A MANE Select	NP_037393.1:p.Ser426Thr
NM_001330751.2:c.1291T>A	NP_001317680.1:p.Ser431Thr
NM_001330752.2:c.1240T>A	NP_001317681.1:p.Ser414Thr
NM_001354825.2:c.1291T>A	NP_001341754.1:p.Ser431Thr
NM_001354826.2:c.895T>A	NP_001341755.1:p.Ser299Thr
NM_001354827.2:c.1291T>A	NP_001341756.1:p.Ser431Thr
NR_148981.2:n.1879T>A
NR_148982.2:n.1952T>A
NR_148983.2:n.2105T>A
NR_148984.2:n.1397T>A
NR_148985.2:n.2017T>A
NR_148986.2:n.2022T>A
NR_148987.2:n.2104T>A
NM_001330753.2:c.895T>A	NP_001317682.1:p.Ser299Thr