Canonical Allele Identifier: CA1444632084

Gene: PPARGC1A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814069C= , CM000666.2:g.23814069C=	GRCh38
NC_000004.11:g.23815692C= , CM000666.1:g.23815692C=	GRCh37
NC_000004.10:g.23424790C=	NCBI36
NG_028250.1:g.81009G=
NG_028250.2:g.663907G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1414G= MANE Select	ENSP00000264867.2:p.Ala472=
ENST00000264867.6:c.1414G=	ENSP00000264867.2:p.Ala472=
ENST00000506055.5:c.*629G=	ENSP00000423075.1:n.*629G=
ENST00000509702.5:n.1454G=
ENST00000613098.4:c.1033G=	ENSP00000481498.1:p.Ala345=
NM_013261.3:c.1414G=	NP_037393.1:p.Ala472=
XM_005248130.2:c.1429G=	XP_005248187.1:p.Ala477=
XM_005248131.3:c.1426G=	XP_005248188.1:p.Ala476=
XM_005248132.1:c.1405G=	XP_005248189.1:p.Ala469=
XM_005248134.3:c.1429G=	XP_005248191.1:p.Ala477=
XM_011513764.1:c.1414G=	XP_011512066.1:p.Ala472=
XM_011513765.1:c.1378G=	XP_011512067.1:p.Ala460=
XM_011513766.1:c.1309G=	XP_011512068.1:p.Ala437=
XM_011513767.1:c.1309G=	XP_011512069.1:p.Ala437=
XM_011513768.1:c.1309G=	XP_011512070.1:p.Ala437=
XM_011513769.1:c.1429G=	XP_011512071.1:p.Ala477=
XM_011513770.1:c.1033G=	XP_011512072.1:p.Ala345=
XM_011513771.1:c.1033G=	XP_011512073.1:p.Ala345=
NM_001330751.1:c.1429G=	NP_001317680.1:p.Ala477=
NM_001330752.1:c.1378G=	NP_001317681.1:p.Ala460=
NM_001330753.1:c.1033G=	NP_001317682.1:p.Ala345=
NM_001354825.1:c.1429G=	NP_001341754.1:p.Ala477=
NM_001354826.1:c.1033G=	NP_001341755.1:p.Ala345=
NM_001354827.1:c.1429G=	NP_001341756.1:p.Ala477=
NM_013261.4:c.1414G=	NP_037393.1:p.Ala472=
NR_148981.1:n.1941G=
NR_148982.1:n.2014G=
NR_148983.1:n.2167G=
NR_148984.1:n.1565G=
NR_148985.1:n.2079G=
NR_148986.1:n.2084G=
NR_148987.1:n.2166G=
XM_005248131.5:c.1426G=	XP_005248188.1:p.Ala476=
XM_005248134.4:c.1429G=	XP_005248191.1:p.Ala477=
XM_011513769.2:c.1429G=	XP_011512071.1:p.Ala477=
XM_024453878.1:c.1429G=	XP_024309646.1:p.Ala477=
NM_013261.5:c.1414G= MANE Select	NP_037393.1:p.Ala472=
NM_001330751.2:c.1429G=	NP_001317680.1:p.Ala477=
NM_001330752.2:c.1378G=	NP_001317681.1:p.Ala460=
NM_001354825.2:c.1429G=	NP_001341754.1:p.Ala477=
NM_001354826.2:c.1033G=	NP_001341755.1:p.Ala345=
NM_001354827.2:c.1429G=	NP_001341756.1:p.Ala477=
NR_148981.2:n.2017G=
NR_148982.2:n.2090G=
NR_148983.2:n.2243G=
NR_148984.2:n.1535G=
NR_148985.2:n.2155G=
NR_148986.2:n.2160G=
NR_148987.2:n.2242G=
NM_001330753.2:c.1033G=	NP_001317682.1:p.Ala345=