Canonical Allele Identifier: CA1444632391

Gene: PPARGC1A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814144A= , CM000666.2:g.23814144A=	GRCh38
NC_000004.11:g.23815767A= , CM000666.1:g.23815767A=	GRCh37
NC_000004.10:g.23424865A=	NCBI36
NG_028250.1:g.80934T=
NG_028250.2:g.663832T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1339T= MANE Select	ENSP00000264867.2:p.Cys447=
ENST00000264867.6:c.1339T=	ENSP00000264867.2:p.Cys447=
ENST00000506055.5:c.*554T=	ENSP00000423075.1:n.*554T=
ENST00000509702.5:n.1379T=
ENST00000613098.4:c.958T=	ENSP00000481498.1:p.Cys320=
NM_013261.3:c.1339T=	NP_037393.1:p.Cys447=
XM_005248130.2:c.1354T=	XP_005248187.1:p.Cys452=
XM_005248131.3:c.1351T=	XP_005248188.1:p.Cys451=
XM_005248132.1:c.1330T=	XP_005248189.1:p.Cys444=
XM_005248134.3:c.1354T=	XP_005248191.1:p.Cys452=
XM_011513764.1:c.1339T=	XP_011512066.1:p.Cys447=
XM_011513765.1:c.1303T=	XP_011512067.1:p.Cys435=
XM_011513766.1:c.1234T=	XP_011512068.1:p.Cys412=
XM_011513767.1:c.1234T=	XP_011512069.1:p.Cys412=
XM_011513768.1:c.1234T=	XP_011512070.1:p.Cys412=
XM_011513769.1:c.1354T=	XP_011512071.1:p.Cys452=
XM_011513770.1:c.958T=	XP_011512072.1:p.Cys320=
XM_011513771.1:c.958T=	XP_011512073.1:p.Cys320=
NM_001330751.1:c.1354T=	NP_001317680.1:p.Cys452=
NM_001330752.1:c.1303T=	NP_001317681.1:p.Cys435=
NM_001330753.1:c.958T=	NP_001317682.1:p.Cys320=
NM_001354825.1:c.1354T=	NP_001341754.1:p.Cys452=
NM_001354826.1:c.958T=	NP_001341755.1:p.Cys320=
NM_001354827.1:c.1354T=	NP_001341756.1:p.Cys452=
NM_013261.4:c.1339T=	NP_037393.1:p.Cys447=
NR_148981.1:n.1866T=
NR_148982.1:n.1939T=
NR_148983.1:n.2092T=
NR_148984.1:n.1490T=
NR_148985.1:n.2004T=
NR_148986.1:n.2009T=
NR_148987.1:n.2091T=
XM_005248131.5:c.1351T=	XP_005248188.1:p.Cys451=
XM_005248134.4:c.1354T=	XP_005248191.1:p.Cys452=
XM_011513769.2:c.1354T=	XP_011512071.1:p.Cys452=
XM_024453878.1:c.1354T=	XP_024309646.1:p.Cys452=
NM_013261.5:c.1339T= MANE Select	NP_037393.1:p.Cys447=
NM_001330751.2:c.1354T=	NP_001317680.1:p.Cys452=
NM_001330752.2:c.1303T=	NP_001317681.1:p.Cys435=
NM_001354825.2:c.1354T=	NP_001341754.1:p.Cys452=
NM_001354826.2:c.958T=	NP_001341755.1:p.Cys320=
NM_001354827.2:c.1354T=	NP_001341756.1:p.Cys452=
NR_148981.2:n.1942T=
NR_148982.2:n.2015T=
NR_148983.2:n.2168T=
NR_148984.2:n.1460T=
NR_148985.2:n.2080T=
NR_148986.2:n.2085T=
NR_148987.2:n.2167T=
NM_001330753.2:c.958T=	NP_001317682.1:p.Cys320=