Canonical Allele Identifier: CA1060212841

Gene: PPARGC1A

Linked Data

• dbSNP Id: rs2970856
• gnomAD v3: 4-23825992-G-C
• gnomAD v4: 4-23825992-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23825992G>C , CM000666.2:g.23825992G>C	GRCh38
NC_000004.11:g.23827615G>C , CM000666.1:g.23827615G>C	GRCh37
NC_000004.10:g.23436713G>C	NCBI36
NG_028250.1:g.69086C>G
NG_028250.2:g.651984C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264867.7:c.758-1484C>G MANE Select	ENSP00000264867.2:n.758-1484C>G
ENST00000264867.6:c.758-1484C>G	ENSP00000264867.2:n.758-1484C>G
ENST00000506055.5:c.758-1484C>G	ENSP00000423075.1:n.758-1484C>G
ENST00000509642.5:n.851-1484C>G
ENST00000509702.5:n.715-743C>G
ENST00000513205.5:c.758-1484C>G	ENSP00000421632.1:n.758-1484C>G
ENST00000612355.1:c.746-1484C>G	ENSP00000479729.1:n.746-1484C>G
ENST00000613098.4:c.377-1484C>G	ENSP00000481498.1:n.377-1484C>G
ENST00000617484.4:c.746-1484C>G	ENSP00000477921.1:n.746-1484C>G
NM_013261.3:c.758-1484C>G	NP_037393.1:n.758-1484C>G
XM_005248130.2:c.773-1484C>G	XP_005248187.1:n.773-1484C>G
XM_005248131.3:c.770-1484C>G	XP_005248188.1:n.770-1484C>G
XM_005248132.1:c.749-1484C>G	XP_005248189.1:n.749-1484C>G
XM_005248134.3:c.773-1484C>G	XP_005248191.1:n.773-1484C>G
XM_011513764.1:c.758-1484C>G	XP_011512066.1:n.758-1484C>G
XM_011513765.1:c.722-1484C>G	XP_011512067.1:n.722-1484C>G
XM_011513766.1:c.653-1484C>G	XP_011512068.1:n.653-1484C>G
XM_011513767.1:c.653-1484C>G	XP_011512069.1:n.653-1484C>G
XM_011513768.1:c.653-1484C>G	XP_011512070.1:n.653-1484C>G
XM_011513769.1:c.773-1484C>G	XP_011512071.1:n.773-1484C>G
XM_011513770.1:c.377-1484C>G	XP_011512072.1:n.377-1484C>G
XM_011513771.1:c.377-1484C>G	XP_011512073.1:n.377-1484C>G
NM_001330751.1:c.773-1484C>G	NP_001317680.1:n.773-1484C>G
NM_001330752.1:c.722-1484C>G	NP_001317681.1:n.722-1484C>G
NM_001330753.1:c.377-1484C>G	NP_001317682.1:n.377-1484C>G
NM_001354825.1:c.773-1484C>G	NP_001341754.1:n.773-1484C>G
NM_001354826.1:c.377-1484C>G	NP_001341755.1:n.377-1484C>G
NM_001354827.1:c.773-1484C>G	NP_001341756.1:n.773-1484C>G
NM_013261.4:c.758-1484C>G	NP_037393.1:n.758-1484C>G
NR_148981.1:n.1285-1484C>G
NR_148982.1:n.1327-1484C>G
NR_148983.1:n.1480-1484C>G
NR_148984.1:n.878-1484C>G
NR_148985.1:n.1392-1484C>G
NR_148986.1:n.1224-1484C>G
NR_148987.1:n.1306-1484C>G
XM_005248131.5:c.770-1484C>G	XP_005248188.1:n.770-1484C>G
XM_005248134.4:c.773-1484C>G	XP_005248191.1:n.773-1484C>G
XM_011513769.2:c.773-1484C>G	XP_011512071.1:n.773-1484C>G
XM_024453878.1:c.773-1484C>G	XP_024309646.1:n.773-1484C>G
NM_013261.5:c.758-1484C>G MANE Select	NP_037393.1:n.758-1484C>G
NM_001330751.2:c.773-1484C>G	NP_001317680.1:n.773-1484C>G
NM_001330752.2:c.722-1484C>G	NP_001317681.1:n.722-1484C>G
NM_001354825.2:c.773-1484C>G	NP_001341754.1:n.773-1484C>G
NM_001354826.2:c.377-1484C>G	NP_001341755.1:n.377-1484C>G
NM_001354827.2:c.773-1484C>G	NP_001341756.1:n.773-1484C>G
NR_148981.2:n.1361-1484C>G
NR_148982.2:n.1403-1484C>G
NR_148983.2:n.1556-1484C>G
NR_148984.2:n.848-1484C>G
NR_148985.2:n.1468-1484C>G
NR_148986.2:n.1300-1484C>G
NR_148987.2:n.1382-1484C>G
NM_001330753.2:c.377-1484C>G	NP_001317682.1:n.377-1484C>G