Canonical Allele Identifier: CA1444632094

Gene: PPARGC1A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814076G= , CM000666.2:g.23814076G=	GRCh38
NC_000004.11:g.23815699G= , CM000666.1:g.23815699G=	GRCh37
NC_000004.10:g.23424797G=	NCBI36
NG_028250.1:g.81002C=
NG_028250.2:g.663900C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1407C= MANE Select	ENSP00000264867.2:p.Pro469=
ENST00000264867.6:c.1407C=	ENSP00000264867.2:p.Pro469=
ENST00000506055.5:c.*622C=	ENSP00000423075.1:n.*622C=
ENST00000509702.5:n.1447C=
ENST00000613098.4:c.1026C=	ENSP00000481498.1:p.Pro342=
NM_013261.3:c.1407C=	NP_037393.1:p.Pro469=
XM_005248130.2:c.1422C=	XP_005248187.1:p.Pro474=
XM_005248131.3:c.1419C=	XP_005248188.1:p.Pro473=
XM_005248132.1:c.1398C=	XP_005248189.1:p.Pro466=
XM_005248134.3:c.1422C=	XP_005248191.1:p.Pro474=
XM_011513764.1:c.1407C=	XP_011512066.1:p.Pro469=
XM_011513765.1:c.1371C=	XP_011512067.1:p.Pro457=
XM_011513766.1:c.1302C=	XP_011512068.1:p.Pro434=
XM_011513767.1:c.1302C=	XP_011512069.1:p.Pro434=
XM_011513768.1:c.1302C=	XP_011512070.1:p.Pro434=
XM_011513769.1:c.1422C=	XP_011512071.1:p.Pro474=
XM_011513770.1:c.1026C=	XP_011512072.1:p.Pro342=
XM_011513771.1:c.1026C=	XP_011512073.1:p.Pro342=
NM_001330751.1:c.1422C=	NP_001317680.1:p.Pro474=
NM_001330752.1:c.1371C=	NP_001317681.1:p.Pro457=
NM_001330753.1:c.1026C=	NP_001317682.1:p.Pro342=
NM_001354825.1:c.1422C=	NP_001341754.1:p.Pro474=
NM_001354826.1:c.1026C=	NP_001341755.1:p.Pro342=
NM_001354827.1:c.1422C=	NP_001341756.1:p.Pro474=
NM_013261.4:c.1407C=	NP_037393.1:p.Pro469=
NR_148981.1:n.1934C=
NR_148982.1:n.2007C=
NR_148983.1:n.2160C=
NR_148984.1:n.1558C=
NR_148985.1:n.2072C=
NR_148986.1:n.2077C=
NR_148987.1:n.2159C=
XM_005248131.5:c.1419C=	XP_005248188.1:p.Pro473=
XM_005248134.4:c.1422C=	XP_005248191.1:p.Pro474=
XM_011513769.2:c.1422C=	XP_011512071.1:p.Pro474=
XM_024453878.1:c.1422C=	XP_024309646.1:p.Pro474=
NM_013261.5:c.1407C= MANE Select	NP_037393.1:p.Pro469=
NM_001330751.2:c.1422C=	NP_001317680.1:p.Pro474=
NM_001330752.2:c.1371C=	NP_001317681.1:p.Pro457=
NM_001354825.2:c.1422C=	NP_001341754.1:p.Pro474=
NM_001354826.2:c.1026C=	NP_001341755.1:p.Pro342=
NM_001354827.2:c.1422C=	NP_001341756.1:p.Pro474=
NR_148981.2:n.2010C=
NR_148982.2:n.2083C=
NR_148983.2:n.2236C=
NR_148984.2:n.1528C=
NR_148985.2:n.2148C=
NR_148986.2:n.2153C=
NR_148987.2:n.2235C=
NM_001330753.2:c.1026C=	NP_001317682.1:p.Pro342=