Canonical Allele Identifier: CA438896276
Gene: PPARGC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.23815840C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23814217C>T , CM000666.2:g.23814217C>T GRCh38
NC_000004.11:g.23815840C>T , CM000666.1:g.23815840C>T GRCh37
NC_000004.10:g.23424938C>T NCBI36
NG_028250.1:g.80861G>A
NG_028250.2:g.663759G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264867.7:c.1266G>A MANE Select ENSP00000264867.2:p.Gln422=
ENST00000264867.6:c.1266G>A ENSP00000264867.2:p.Gln422=
ENST00000506055.5:c.*481G>A ENSP00000423075.1:n.*481G>A
ENST00000509702.5:n.1306G>A
ENST00000613098.4:c.885G>A ENSP00000481498.1:p.Gln295=
NM_013261.3:c.1266G>A NP_037393.1:p.Gln422=
XM_005248130.2:c.1281G>A XP_005248187.1:p.Gln427=
XM_005248131.3:c.1278G>A XP_005248188.1:p.Gln426=
XM_005248132.1:c.1257G>A XP_005248189.1:p.Gln419=
XM_005248134.3:c.1281G>A XP_005248191.1:p.Gln427=
XM_011513764.1:c.1266G>A XP_011512066.1:p.Gln422=
XM_011513765.1:c.1230G>A XP_011512067.1:p.Gln410=
XM_011513766.1:c.1161G>A XP_011512068.1:p.Gln387=
XM_011513767.1:c.1161G>A XP_011512069.1:p.Gln387=
XM_011513768.1:c.1161G>A XP_011512070.1:p.Gln387=
XM_011513769.1:c.1281G>A XP_011512071.1:p.Gln427=
XM_011513770.1:c.885G>A XP_011512072.1:p.Gln295=
XM_011513771.1:c.885G>A XP_011512073.1:p.Gln295=
NM_001330751.1:c.1281G>A NP_001317680.1:p.Gln427=
NM_001330752.1:c.1230G>A NP_001317681.1:p.Gln410=
NM_001330753.1:c.885G>A NP_001317682.1:p.Gln295=
NM_001354825.1:c.1281G>A NP_001341754.1:p.Gln427=
NM_001354826.1:c.885G>A NP_001341755.1:p.Gln295=
NM_001354827.1:c.1281G>A NP_001341756.1:p.Gln427=
NM_013261.4:c.1266G>A NP_037393.1:p.Gln422=
NR_148981.1:n.1793G>A
NR_148982.1:n.1866G>A
NR_148983.1:n.2019G>A
NR_148984.1:n.1417G>A
NR_148985.1:n.1931G>A
NR_148986.1:n.1936G>A
NR_148987.1:n.2018G>A
XM_005248131.5:c.1278G>A XP_005248188.1:p.Gln426=
XM_005248134.4:c.1281G>A XP_005248191.1:p.Gln427=
XM_011513769.2:c.1281G>A XP_011512071.1:p.Gln427=
XM_024453878.1:c.1281G>A XP_024309646.1:p.Gln427=
NM_013261.5:c.1266G>A MANE Select NP_037393.1:p.Gln422=
NM_001330751.2:c.1281G>A NP_001317680.1:p.Gln427=
NM_001330752.2:c.1230G>A NP_001317681.1:p.Gln410=
NM_001354825.2:c.1281G>A NP_001341754.1:p.Gln427=
NM_001354826.2:c.885G>A NP_001341755.1:p.Gln295=
NM_001354827.2:c.1281G>A NP_001341756.1:p.Gln427=
NR_148981.2:n.1869G>A
NR_148982.2:n.1942G>A
NR_148983.2:n.2095G>A
NR_148984.2:n.1387G>A
NR_148985.2:n.2007G>A
NR_148986.2:n.2012G>A
NR_148987.2:n.2094G>A
NM_001330753.2:c.885G>A NP_001317682.1:p.Gln295=