Canonical Allele Identifier: CA914920698

Gene: PPARGC1A

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23815404A>C , CM000666.2:g.23815404A>C	GRCh38
NC_000004.11:g.23817027A>C , CM000666.1:g.23817027A>C	GRCh37
NC_000004.10:g.23426125A>C	NCBI36
NG_028250.1:g.79674T>G
NG_028250.2:g.662572T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.878-799T>G MANE Select	ENSP00000264867.2:n.878-799T>G
ENST00000264867.6:c.878-799T>G	ENSP00000264867.2:n.878-799T>G
ENST00000506055.5:c.*93-799T>G	ENSP00000423075.1:n.*93-799T>G
ENST00000509642.5:n.1175-799T>G
ENST00000509702.5:n.918-799T>G
ENST00000513205.5:c.*176-799T>G	ENSP00000421632.1:n.*176-799T>G
ENST00000613098.4:c.497-799T>G	ENSP00000481498.1:n.497-799T>G
NM_013261.3:c.878-799T>G	NP_037393.1:n.878-799T>G
XM_005248130.2:c.893-799T>G	XP_005248187.1:n.893-799T>G
XM_005248131.3:c.890-799T>G	XP_005248188.1:n.890-799T>G
XM_005248132.1:c.869-799T>G	XP_005248189.1:n.869-799T>G
XM_005248134.3:c.893-799T>G	XP_005248191.1:n.893-799T>G
XM_011513764.1:c.878-799T>G	XP_011512066.1:n.878-799T>G
XM_011513765.1:c.842-799T>G	XP_011512067.1:n.842-799T>G
XM_011513766.1:c.773-799T>G	XP_011512068.1:n.773-799T>G
XM_011513767.1:c.773-799T>G	XP_011512069.1:n.773-799T>G
XM_011513768.1:c.773-799T>G	XP_011512070.1:n.773-799T>G
XM_011513769.1:c.893-799T>G	XP_011512071.1:n.893-799T>G
XM_011513770.1:c.497-799T>G	XP_011512072.1:n.497-799T>G
XM_011513771.1:c.497-799T>G	XP_011512073.1:n.497-799T>G
NM_001330751.1:c.893-799T>G	NP_001317680.1:n.893-799T>G
NM_001330752.1:c.842-799T>G	NP_001317681.1:n.842-799T>G
NM_001330753.1:c.497-799T>G	NP_001317682.1:n.497-799T>G
NM_001354825.1:c.893-799T>G	NP_001341754.1:n.893-799T>G
NM_001354826.1:c.497-799T>G	NP_001341755.1:n.497-799T>G
NM_001354827.1:c.893-799T>G	NP_001341756.1:n.893-799T>G
NM_013261.4:c.878-799T>G	NP_037393.1:n.878-799T>G
NR_148981.1:n.1405-799T>G
NR_148982.1:n.1478-799T>G
NR_148983.1:n.1631-799T>G
NR_148984.1:n.1029-799T>G
NR_148985.1:n.1543-799T>G
NR_148986.1:n.1548-799T>G
NR_148987.1:n.1630-799T>G
XM_005248131.5:c.890-799T>G	XP_005248188.1:n.890-799T>G
XM_005248134.4:c.893-799T>G	XP_005248191.1:n.893-799T>G
XM_011513769.2:c.893-799T>G	XP_011512071.1:n.893-799T>G
XM_024453878.1:c.893-799T>G	XP_024309646.1:n.893-799T>G
NM_013261.5:c.878-799T>G MANE Select	NP_037393.1:n.878-799T>G
NM_001330751.2:c.893-799T>G	NP_001317680.1:n.893-799T>G
NM_001330752.2:c.842-799T>G	NP_001317681.1:n.842-799T>G
NM_001354825.2:c.893-799T>G	NP_001341754.1:n.893-799T>G
NM_001354826.2:c.497-799T>G	NP_001341755.1:n.497-799T>G
NM_001354827.2:c.893-799T>G	NP_001341756.1:n.893-799T>G
NR_148981.2:n.1481-799T>G
NR_148982.2:n.1554-799T>G
NR_148983.2:n.1707-799T>G
NR_148984.2:n.999-799T>G
NR_148985.2:n.1619-799T>G
NR_148986.2:n.1624-799T>G
NR_148987.2:n.1706-799T>G
NM_001330753.2:c.497-799T>G	NP_001317682.1:n.497-799T>G