Canonical Allele Identifier: CA1444632443

Gene: PPARGC1A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814179C= , CM000666.2:g.23814179C=	GRCh38
NC_000004.11:g.23815802C= , CM000666.1:g.23815802C=	GRCh37
NC_000004.10:g.23424900C=	NCBI36
NG_028250.1:g.80899G=
NG_028250.2:g.663797G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1304G= MANE Select	ENSP00000264867.2:p.Arg435=
ENST00000264867.6:c.1304G=	ENSP00000264867.2:p.Arg435=
ENST00000506055.5:c.*519G=	ENSP00000423075.1:n.*519G=
ENST00000509702.5:n.1344G=
ENST00000613098.4:c.923G=	ENSP00000481498.1:p.Arg308=
NM_013261.3:c.1304G=	NP_037393.1:p.Arg435=
XM_005248130.2:c.1319G=	XP_005248187.1:p.Arg440=
XM_005248131.3:c.1316G=	XP_005248188.1:p.Arg439=
XM_005248132.1:c.1295G=	XP_005248189.1:p.Arg432=
XM_005248134.3:c.1319G=	XP_005248191.1:p.Arg440=
XM_011513764.1:c.1304G=	XP_011512066.1:p.Arg435=
XM_011513765.1:c.1268G=	XP_011512067.1:p.Arg423=
XM_011513766.1:c.1199G=	XP_011512068.1:p.Arg400=
XM_011513767.1:c.1199G=	XP_011512069.1:p.Arg400=
XM_011513768.1:c.1199G=	XP_011512070.1:p.Arg400=
XM_011513769.1:c.1319G=	XP_011512071.1:p.Arg440=
XM_011513770.1:c.923G=	XP_011512072.1:p.Arg308=
XM_011513771.1:c.923G=	XP_011512073.1:p.Arg308=
NM_001330751.1:c.1319G=	NP_001317680.1:p.Arg440=
NM_001330752.1:c.1268G=	NP_001317681.1:p.Arg423=
NM_001330753.1:c.923G=	NP_001317682.1:p.Arg308=
NM_001354825.1:c.1319G=	NP_001341754.1:p.Arg440=
NM_001354826.1:c.923G=	NP_001341755.1:p.Arg308=
NM_001354827.1:c.1319G=	NP_001341756.1:p.Arg440=
NM_013261.4:c.1304G=	NP_037393.1:p.Arg435=
NR_148981.1:n.1831G=
NR_148982.1:n.1904G=
NR_148983.1:n.2057G=
NR_148984.1:n.1455G=
NR_148985.1:n.1969G=
NR_148986.1:n.1974G=
NR_148987.1:n.2056G=
XM_005248131.5:c.1316G=	XP_005248188.1:p.Arg439=
XM_005248134.4:c.1319G=	XP_005248191.1:p.Arg440=
XM_011513769.2:c.1319G=	XP_011512071.1:p.Arg440=
XM_024453878.1:c.1319G=	XP_024309646.1:p.Arg440=
NM_013261.5:c.1304G= MANE Select	NP_037393.1:p.Arg435=
NM_001330751.2:c.1319G=	NP_001317680.1:p.Arg440=
NM_001330752.2:c.1268G=	NP_001317681.1:p.Arg423=
NM_001354825.2:c.1319G=	NP_001341754.1:p.Arg440=
NM_001354826.2:c.923G=	NP_001341755.1:p.Arg308=
NM_001354827.2:c.1319G=	NP_001341756.1:p.Arg440=
NR_148981.2:n.1907G=
NR_148982.2:n.1980G=
NR_148983.2:n.2133G=
NR_148984.2:n.1425G=
NR_148985.2:n.2045G=
NR_148986.2:n.2050G=
NR_148987.2:n.2132G=
NM_001330753.2:c.923G=	NP_001317682.1:p.Arg308=