Canonical Allele Identifier: CA1444632371

Gene: PPARGC1A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814127C= , CM000666.2:g.23814127C=	GRCh38
NC_000004.11:g.23815750C= , CM000666.1:g.23815750C=	GRCh37
NC_000004.10:g.23424848C=	NCBI36
NG_028250.1:g.80951G=
NG_028250.2:g.663849G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1356G= MANE Select	ENSP00000264867.2:p.Gln452=
ENST00000264867.6:c.1356G=	ENSP00000264867.2:p.Gln452=
ENST00000506055.5:c.*571G=	ENSP00000423075.1:n.*571G=
ENST00000509702.5:n.1396G=
ENST00000613098.4:c.975G=	ENSP00000481498.1:p.Gln325=
NM_013261.3:c.1356G=	NP_037393.1:p.Gln452=
XM_005248130.2:c.1371G=	XP_005248187.1:p.Gln457=
XM_005248131.3:c.1368G=	XP_005248188.1:p.Gln456=
XM_005248132.1:c.1347G=	XP_005248189.1:p.Gln449=
XM_005248134.3:c.1371G=	XP_005248191.1:p.Gln457=
XM_011513764.1:c.1356G=	XP_011512066.1:p.Gln452=
XM_011513765.1:c.1320G=	XP_011512067.1:p.Gln440=
XM_011513766.1:c.1251G=	XP_011512068.1:p.Gln417=
XM_011513767.1:c.1251G=	XP_011512069.1:p.Gln417=
XM_011513768.1:c.1251G=	XP_011512070.1:p.Gln417=
XM_011513769.1:c.1371G=	XP_011512071.1:p.Gln457=
XM_011513770.1:c.975G=	XP_011512072.1:p.Gln325=
XM_011513771.1:c.975G=	XP_011512073.1:p.Gln325=
NM_001330751.1:c.1371G=	NP_001317680.1:p.Gln457=
NM_001330752.1:c.1320G=	NP_001317681.1:p.Gln440=
NM_001330753.1:c.975G=	NP_001317682.1:p.Gln325=
NM_001354825.1:c.1371G=	NP_001341754.1:p.Gln457=
NM_001354826.1:c.975G=	NP_001341755.1:p.Gln325=
NM_001354827.1:c.1371G=	NP_001341756.1:p.Gln457=
NM_013261.4:c.1356G=	NP_037393.1:p.Gln452=
NR_148981.1:n.1883G=
NR_148982.1:n.1956G=
NR_148983.1:n.2109G=
NR_148984.1:n.1507G=
NR_148985.1:n.2021G=
NR_148986.1:n.2026G=
NR_148987.1:n.2108G=
XM_005248131.5:c.1368G=	XP_005248188.1:p.Gln456=
XM_005248134.4:c.1371G=	XP_005248191.1:p.Gln457=
XM_011513769.2:c.1371G=	XP_011512071.1:p.Gln457=
XM_024453878.1:c.1371G=	XP_024309646.1:p.Gln457=
NM_013261.5:c.1356G= MANE Select	NP_037393.1:p.Gln452=
NM_001330751.2:c.1371G=	NP_001317680.1:p.Gln457=
NM_001330752.2:c.1320G=	NP_001317681.1:p.Gln440=
NM_001354825.2:c.1371G=	NP_001341754.1:p.Gln457=
NM_001354826.2:c.975G=	NP_001341755.1:p.Gln325=
NM_001354827.2:c.1371G=	NP_001341756.1:p.Gln457=
NR_148981.2:n.1959G=
NR_148982.2:n.2032G=
NR_148983.2:n.2185G=
NR_148984.2:n.1477G=
NR_148985.2:n.2097G=
NR_148986.2:n.2102G=
NR_148987.2:n.2184G=
NM_001330753.2:c.975G=	NP_001317682.1:p.Gln325=