Canonical Allele Identifier: CA356524553

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815796G>A (hg19) ; chr4:g.23814173G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814173G>A , CM000666.2:g.23814173G>A	GRCh38
NC_000004.11:g.23815796G>A , CM000666.1:g.23815796G>A	GRCh37
NC_000004.10:g.23424894G>A	NCBI36
NG_028250.1:g.80905C>T
NG_028250.2:g.663803C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1310C>T MANE Select	ENSP00000264867.2:p.Thr437Ile
ENST00000264867.6:c.1310C>T	ENSP00000264867.2:p.Thr437Ile
ENST00000506055.5:c.*525C>T	ENSP00000423075.1:n.*525C>T
ENST00000509702.5:n.1350C>T
ENST00000613098.4:c.929C>T	ENSP00000481498.1:p.Thr310Ile
NM_013261.3:c.1310C>T	NP_037393.1:p.Thr437Ile
XM_005248130.2:c.1325C>T	XP_005248187.1:p.Thr442Ile
XM_005248131.3:c.1322C>T	XP_005248188.1:p.Thr441Ile
XM_005248132.1:c.1301C>T	XP_005248189.1:p.Thr434Ile
XM_005248134.3:c.1325C>T	XP_005248191.1:p.Thr442Ile
XM_011513764.1:c.1310C>T	XP_011512066.1:p.Thr437Ile
XM_011513765.1:c.1274C>T	XP_011512067.1:p.Thr425Ile
XM_011513766.1:c.1205C>T	XP_011512068.1:p.Thr402Ile
XM_011513767.1:c.1205C>T	XP_011512069.1:p.Thr402Ile
XM_011513768.1:c.1205C>T	XP_011512070.1:p.Thr402Ile
XM_011513769.1:c.1325C>T	XP_011512071.1:p.Thr442Ile
XM_011513770.1:c.929C>T	XP_011512072.1:p.Thr310Ile
XM_011513771.1:c.929C>T	XP_011512073.1:p.Thr310Ile
NM_001330751.1:c.1325C>T	NP_001317680.1:p.Thr442Ile
NM_001330752.1:c.1274C>T	NP_001317681.1:p.Thr425Ile
NM_001330753.1:c.929C>T	NP_001317682.1:p.Thr310Ile
NM_001354825.1:c.1325C>T	NP_001341754.1:p.Thr442Ile
NM_001354826.1:c.929C>T	NP_001341755.1:p.Thr310Ile
NM_001354827.1:c.1325C>T	NP_001341756.1:p.Thr442Ile
NM_013261.4:c.1310C>T	NP_037393.1:p.Thr437Ile
NR_148981.1:n.1837C>T
NR_148982.1:n.1910C>T
NR_148983.1:n.2063C>T
NR_148984.1:n.1461C>T
NR_148985.1:n.1975C>T
NR_148986.1:n.1980C>T
NR_148987.1:n.2062C>T
XM_005248131.5:c.1322C>T	XP_005248188.1:p.Thr441Ile
XM_005248134.4:c.1325C>T	XP_005248191.1:p.Thr442Ile
XM_011513769.2:c.1325C>T	XP_011512071.1:p.Thr442Ile
XM_024453878.1:c.1325C>T	XP_024309646.1:p.Thr442Ile
NM_013261.5:c.1310C>T MANE Select	NP_037393.1:p.Thr437Ile
NM_001330751.2:c.1325C>T	NP_001317680.1:p.Thr442Ile
NM_001330752.2:c.1274C>T	NP_001317681.1:p.Thr425Ile
NM_001354825.2:c.1325C>T	NP_001341754.1:p.Thr442Ile
NM_001354826.2:c.929C>T	NP_001341755.1:p.Thr310Ile
NM_001354827.2:c.1325C>T	NP_001341756.1:p.Thr442Ile
NR_148981.2:n.1913C>T
NR_148982.2:n.1986C>T
NR_148983.2:n.2139C>T
NR_148984.2:n.1431C>T
NR_148985.2:n.2051C>T
NR_148986.2:n.2056C>T
NR_148987.2:n.2138C>T
NM_001330753.2:c.929C>T	NP_001317682.1:p.Thr310Ile