Canonical Allele Identifier: CA356524319

Gene: PPARGC1A

Linked Data

• dbSNP Id: rs755845144
• gnomAD v2: 4-23815692-C-A
• gnomAD v4: 4-23814069-C-A
• MyVariant Identifiers: chr4:g.23815692C>A (hg19) ; chr4:g.23814069C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814069C>A , CM000666.2:g.23814069C>A	GRCh38
NC_000004.11:g.23815692C>A , CM000666.1:g.23815692C>A	GRCh37
NC_000004.10:g.23424790C>A	NCBI36
NG_028250.1:g.81009G>T
NG_028250.2:g.663907G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1414G>T MANE Select	ENSP00000264867.2:p.Ala472Ser
ENST00000264867.6:c.1414G>T	ENSP00000264867.2:p.Ala472Ser
ENST00000506055.5:c.*629G>T	ENSP00000423075.1:n.*629G>T
ENST00000509702.5:n.1454G>T
ENST00000613098.4:c.1033G>T	ENSP00000481498.1:p.Ala345Ser
NM_013261.3:c.1414G>T	NP_037393.1:p.Ala472Ser
XM_005248130.2:c.1429G>T	XP_005248187.1:p.Ala477Ser
XM_005248131.3:c.1426G>T	XP_005248188.1:p.Ala476Ser
XM_005248132.1:c.1405G>T	XP_005248189.1:p.Ala469Ser
XM_005248134.3:c.1429G>T	XP_005248191.1:p.Ala477Ser
XM_011513764.1:c.1414G>T	XP_011512066.1:p.Ala472Ser
XM_011513765.1:c.1378G>T	XP_011512067.1:p.Ala460Ser
XM_011513766.1:c.1309G>T	XP_011512068.1:p.Ala437Ser
XM_011513767.1:c.1309G>T	XP_011512069.1:p.Ala437Ser
XM_011513768.1:c.1309G>T	XP_011512070.1:p.Ala437Ser
XM_011513769.1:c.1429G>T	XP_011512071.1:p.Ala477Ser
XM_011513770.1:c.1033G>T	XP_011512072.1:p.Ala345Ser
XM_011513771.1:c.1033G>T	XP_011512073.1:p.Ala345Ser
NM_001330751.1:c.1429G>T	NP_001317680.1:p.Ala477Ser
NM_001330752.1:c.1378G>T	NP_001317681.1:p.Ala460Ser
NM_001330753.1:c.1033G>T	NP_001317682.1:p.Ala345Ser
NM_001354825.1:c.1429G>T	NP_001341754.1:p.Ala477Ser
NM_001354826.1:c.1033G>T	NP_001341755.1:p.Ala345Ser
NM_001354827.1:c.1429G>T	NP_001341756.1:p.Ala477Ser
NM_013261.4:c.1414G>T	NP_037393.1:p.Ala472Ser
NR_148981.1:n.1941G>T
NR_148982.1:n.2014G>T
NR_148983.1:n.2167G>T
NR_148984.1:n.1565G>T
NR_148985.1:n.2079G>T
NR_148986.1:n.2084G>T
NR_148987.1:n.2166G>T
XM_005248131.5:c.1426G>T	XP_005248188.1:p.Ala476Ser
XM_005248134.4:c.1429G>T	XP_005248191.1:p.Ala477Ser
XM_011513769.2:c.1429G>T	XP_011512071.1:p.Ala477Ser
XM_024453878.1:c.1429G>T	XP_024309646.1:p.Ala477Ser
NM_013261.5:c.1414G>T MANE Select	NP_037393.1:p.Ala472Ser
NM_001330751.2:c.1429G>T	NP_001317680.1:p.Ala477Ser
NM_001330752.2:c.1378G>T	NP_001317681.1:p.Ala460Ser
NM_001354825.2:c.1429G>T	NP_001341754.1:p.Ala477Ser
NM_001354826.2:c.1033G>T	NP_001341755.1:p.Ala345Ser
NM_001354827.2:c.1429G>T	NP_001341756.1:p.Ala477Ser
NR_148981.2:n.2017G>T
NR_148982.2:n.2090G>T
NR_148983.2:n.2243G>T
NR_148984.2:n.1535G>T
NR_148985.2:n.2155G>T
NR_148986.2:n.2160G>T
NR_148987.2:n.2242G>T
NM_001330753.2:c.1033G>T	NP_001317682.1:p.Ala345Ser