Canonical Allele Identifier: CA356524507

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815775A>T (hg19) ; chr4:g.23814152A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814152A>T , CM000666.2:g.23814152A>T	GRCh38
NC_000004.11:g.23815775A>T , CM000666.1:g.23815775A>T	GRCh37
NC_000004.10:g.23424873A>T	NCBI36
NG_028250.1:g.80926T>A
NG_028250.2:g.663824T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1331T>A MANE Select	ENSP00000264867.2:p.Val444Asp
ENST00000264867.6:c.1331T>A	ENSP00000264867.2:p.Val444Asp
ENST00000506055.5:c.*546T>A	ENSP00000423075.1:n.*546T>A
ENST00000509702.5:n.1371T>A
ENST00000613098.4:c.950T>A	ENSP00000481498.1:p.Val317Asp
NM_013261.3:c.1331T>A	NP_037393.1:p.Val444Asp
XM_005248130.2:c.1346T>A	XP_005248187.1:p.Val449Asp
XM_005248131.3:c.1343T>A	XP_005248188.1:p.Val448Asp
XM_005248132.1:c.1322T>A	XP_005248189.1:p.Val441Asp
XM_005248134.3:c.1346T>A	XP_005248191.1:p.Val449Asp
XM_011513764.1:c.1331T>A	XP_011512066.1:p.Val444Asp
XM_011513765.1:c.1295T>A	XP_011512067.1:p.Val432Asp
XM_011513766.1:c.1226T>A	XP_011512068.1:p.Val409Asp
XM_011513767.1:c.1226T>A	XP_011512069.1:p.Val409Asp
XM_011513768.1:c.1226T>A	XP_011512070.1:p.Val409Asp
XM_011513769.1:c.1346T>A	XP_011512071.1:p.Val449Asp
XM_011513770.1:c.950T>A	XP_011512072.1:p.Val317Asp
XM_011513771.1:c.950T>A	XP_011512073.1:p.Val317Asp
NM_001330751.1:c.1346T>A	NP_001317680.1:p.Val449Asp
NM_001330752.1:c.1295T>A	NP_001317681.1:p.Val432Asp
NM_001330753.1:c.950T>A	NP_001317682.1:p.Val317Asp
NM_001354825.1:c.1346T>A	NP_001341754.1:p.Val449Asp
NM_001354826.1:c.950T>A	NP_001341755.1:p.Val317Asp
NM_001354827.1:c.1346T>A	NP_001341756.1:p.Val449Asp
NM_013261.4:c.1331T>A	NP_037393.1:p.Val444Asp
NR_148981.1:n.1858T>A
NR_148982.1:n.1931T>A
NR_148983.1:n.2084T>A
NR_148984.1:n.1482T>A
NR_148985.1:n.1996T>A
NR_148986.1:n.2001T>A
NR_148987.1:n.2083T>A
XM_005248131.5:c.1343T>A	XP_005248188.1:p.Val448Asp
XM_005248134.4:c.1346T>A	XP_005248191.1:p.Val449Asp
XM_011513769.2:c.1346T>A	XP_011512071.1:p.Val449Asp
XM_024453878.1:c.1346T>A	XP_024309646.1:p.Val449Asp
NM_013261.5:c.1331T>A MANE Select	NP_037393.1:p.Val444Asp
NM_001330751.2:c.1346T>A	NP_001317680.1:p.Val449Asp
NM_001330752.2:c.1295T>A	NP_001317681.1:p.Val432Asp
NM_001354825.2:c.1346T>A	NP_001341754.1:p.Val449Asp
NM_001354826.2:c.950T>A	NP_001341755.1:p.Val317Asp
NM_001354827.2:c.1346T>A	NP_001341756.1:p.Val449Asp
NR_148981.2:n.1934T>A
NR_148982.2:n.2007T>A
NR_148983.2:n.2160T>A
NR_148984.2:n.1452T>A
NR_148985.2:n.2072T>A
NR_148986.2:n.2077T>A
NR_148987.2:n.2159T>A
NM_001330753.2:c.950T>A	NP_001317682.1:p.Val317Asp