Canonical Allele Identifier: CA356524693

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815841T>G (hg19) ; chr4:g.23814218T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814218T>G , CM000666.2:g.23814218T>G	GRCh38
NC_000004.11:g.23815841T>G , CM000666.1:g.23815841T>G	GRCh37
NC_000004.10:g.23424939T>G	NCBI36
NG_028250.1:g.80860A>C
NG_028250.2:g.663758A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1265A>C MANE Select	ENSP00000264867.2:p.Gln422Pro
ENST00000264867.6:c.1265A>C	ENSP00000264867.2:p.Gln422Pro
ENST00000506055.5:c.*480A>C	ENSP00000423075.1:n.*480A>C
ENST00000509702.5:n.1305A>C
ENST00000613098.4:c.884A>C	ENSP00000481498.1:p.Gln295Pro
NM_013261.3:c.1265A>C	NP_037393.1:p.Gln422Pro
XM_005248130.2:c.1280A>C	XP_005248187.1:p.Gln427Pro
XM_005248131.3:c.1277A>C	XP_005248188.1:p.Gln426Pro
XM_005248132.1:c.1256A>C	XP_005248189.1:p.Gln419Pro
XM_005248134.3:c.1280A>C	XP_005248191.1:p.Gln427Pro
XM_011513764.1:c.1265A>C	XP_011512066.1:p.Gln422Pro
XM_011513765.1:c.1229A>C	XP_011512067.1:p.Gln410Pro
XM_011513766.1:c.1160A>C	XP_011512068.1:p.Gln387Pro
XM_011513767.1:c.1160A>C	XP_011512069.1:p.Gln387Pro
XM_011513768.1:c.1160A>C	XP_011512070.1:p.Gln387Pro
XM_011513769.1:c.1280A>C	XP_011512071.1:p.Gln427Pro
XM_011513770.1:c.884A>C	XP_011512072.1:p.Gln295Pro
XM_011513771.1:c.884A>C	XP_011512073.1:p.Gln295Pro
NM_001330751.1:c.1280A>C	NP_001317680.1:p.Gln427Pro
NM_001330752.1:c.1229A>C	NP_001317681.1:p.Gln410Pro
NM_001330753.1:c.884A>C	NP_001317682.1:p.Gln295Pro
NM_001354825.1:c.1280A>C	NP_001341754.1:p.Gln427Pro
NM_001354826.1:c.884A>C	NP_001341755.1:p.Gln295Pro
NM_001354827.1:c.1280A>C	NP_001341756.1:p.Gln427Pro
NM_013261.4:c.1265A>C	NP_037393.1:p.Gln422Pro
NR_148981.1:n.1792A>C
NR_148982.1:n.1865A>C
NR_148983.1:n.2018A>C
NR_148984.1:n.1416A>C
NR_148985.1:n.1930A>C
NR_148986.1:n.1935A>C
NR_148987.1:n.2017A>C
XM_005248131.5:c.1277A>C	XP_005248188.1:p.Gln426Pro
XM_005248134.4:c.1280A>C	XP_005248191.1:p.Gln427Pro
XM_011513769.2:c.1280A>C	XP_011512071.1:p.Gln427Pro
XM_024453878.1:c.1280A>C	XP_024309646.1:p.Gln427Pro
NM_013261.5:c.1265A>C MANE Select	NP_037393.1:p.Gln422Pro
NM_001330751.2:c.1280A>C	NP_001317680.1:p.Gln427Pro
NM_001330752.2:c.1229A>C	NP_001317681.1:p.Gln410Pro
NM_001354825.2:c.1280A>C	NP_001341754.1:p.Gln427Pro
NM_001354826.2:c.884A>C	NP_001341755.1:p.Gln295Pro
NM_001354827.2:c.1280A>C	NP_001341756.1:p.Gln427Pro
NR_148981.2:n.1868A>C
NR_148982.2:n.1941A>C
NR_148983.2:n.2094A>C
NR_148984.2:n.1386A>C
NR_148985.2:n.2006A>C
NR_148986.2:n.2011A>C
NR_148987.2:n.2093A>C
NM_001330753.2:c.884A>C	NP_001317682.1:p.Gln295Pro