Canonical Allele Identifier: CA2875281

Gene: PPARGC1A

Linked Data

• ClinVar Variation Id: 745082
• ClinVar RCV Id: RCV000921587
• dbSNP Id: rs759025415
• ExAC: 4:23815843 C / T
• gnomAD v2: 4-23815843-C-T
• gnomAD v3: 4-23814220-C-T
• gnomAD v4: 4-23814220-C-T
• MyVariant Identifiers: chr4:g.23815843C>T (hg19) ; chr4:g.23814220C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814220C>T , CM000666.2:g.23814220C>T	GRCh38
NC_000004.11:g.23815843C>T , CM000666.1:g.23815843C>T	GRCh37
NC_000004.10:g.23424941C>T	NCBI36
NG_028250.1:g.80858G>A
NG_028250.2:g.663756G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1263G>A MANE Select	ENSP00000264867.2:p.Gly421=
ENST00000264867.6:c.1263G>A	ENSP00000264867.2:p.Gly421=
ENST00000506055.5:c.*478G>A	ENSP00000423075.1:n.*478G>A
ENST00000509702.5:n.1303G>A
ENST00000613098.4:c.882G>A	ENSP00000481498.1:p.Gly294=
NM_013261.3:c.1263G>A	NP_037393.1:p.Gly421=
XM_005248130.2:c.1278G>A	XP_005248187.1:p.Gly426=
XM_005248131.3:c.1275G>A	XP_005248188.1:p.Gly425=
XM_005248132.1:c.1254G>A	XP_005248189.1:p.Gly418=
XM_005248134.3:c.1278G>A	XP_005248191.1:p.Gly426=
XM_011513764.1:c.1263G>A	XP_011512066.1:p.Gly421=
XM_011513765.1:c.1227G>A	XP_011512067.1:p.Gly409=
XM_011513766.1:c.1158G>A	XP_011512068.1:p.Gly386=
XM_011513767.1:c.1158G>A	XP_011512069.1:p.Gly386=
XM_011513768.1:c.1158G>A	XP_011512070.1:p.Gly386=
XM_011513769.1:c.1278G>A	XP_011512071.1:p.Gly426=
XM_011513770.1:c.882G>A	XP_011512072.1:p.Gly294=
XM_011513771.1:c.882G>A	XP_011512073.1:p.Gly294=
NM_001330751.1:c.1278G>A	NP_001317680.1:p.Gly426=
NM_001330752.1:c.1227G>A	NP_001317681.1:p.Gly409=
NM_001330753.1:c.882G>A	NP_001317682.1:p.Gly294=
NM_001354825.1:c.1278G>A	NP_001341754.1:p.Gly426=
NM_001354826.1:c.882G>A	NP_001341755.1:p.Gly294=
NM_001354827.1:c.1278G>A	NP_001341756.1:p.Gly426=
NM_013261.4:c.1263G>A	NP_037393.1:p.Gly421=
NR_148981.1:n.1790G>A
NR_148982.1:n.1863G>A
NR_148983.1:n.2016G>A
NR_148984.1:n.1414G>A
NR_148985.1:n.1928G>A
NR_148986.1:n.1933G>A
NR_148987.1:n.2015G>A
XM_005248131.5:c.1275G>A	XP_005248188.1:p.Gly425=
XM_005248134.4:c.1278G>A	XP_005248191.1:p.Gly426=
XM_011513769.2:c.1278G>A	XP_011512071.1:p.Gly426=
XM_024453878.1:c.1278G>A	XP_024309646.1:p.Gly426=
NM_013261.5:c.1263G>A MANE Select	NP_037393.1:p.Gly421=
NM_001330751.2:c.1278G>A	NP_001317680.1:p.Gly426=
NM_001330752.2:c.1227G>A	NP_001317681.1:p.Gly409=
NM_001354825.2:c.1278G>A	NP_001341754.1:p.Gly426=
NM_001354826.2:c.882G>A	NP_001341755.1:p.Gly294=
NM_001354827.2:c.1278G>A	NP_001341756.1:p.Gly426=
NR_148981.2:n.1866G>A
NR_148982.2:n.1939G>A
NR_148983.2:n.2092G>A
NR_148984.2:n.1384G>A
NR_148985.2:n.2004G>A
NR_148986.2:n.2009G>A
NR_148987.2:n.2091G>A
NM_001330753.2:c.882G>A	NP_001317682.1:p.Gly294=