Canonical Allele Identifier: CA356524679

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815837A>C (hg19) ; chr4:g.23814214A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814214A>C , CM000666.2:g.23814214A>C	GRCh38
NC_000004.11:g.23815837A>C , CM000666.1:g.23815837A>C	GRCh37
NC_000004.10:g.23424935A>C	NCBI36
NG_028250.1:g.80864T>G
NG_028250.2:g.663762T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1269T>G MANE Select	ENSP00000264867.2:p.Ile423Met
ENST00000264867.6:c.1269T>G	ENSP00000264867.2:p.Ile423Met
ENST00000506055.5:c.*484T>G	ENSP00000423075.1:n.*484T>G
ENST00000509702.5:n.1309T>G
ENST00000613098.4:c.888T>G	ENSP00000481498.1:p.Ile296Met
NM_013261.3:c.1269T>G	NP_037393.1:p.Ile423Met
XM_005248130.2:c.1284T>G	XP_005248187.1:p.Ile428Met
XM_005248131.3:c.1281T>G	XP_005248188.1:p.Ile427Met
XM_005248132.1:c.1260T>G	XP_005248189.1:p.Ile420Met
XM_005248134.3:c.1284T>G	XP_005248191.1:p.Ile428Met
XM_011513764.1:c.1269T>G	XP_011512066.1:p.Ile423Met
XM_011513765.1:c.1233T>G	XP_011512067.1:p.Ile411Met
XM_011513766.1:c.1164T>G	XP_011512068.1:p.Ile388Met
XM_011513767.1:c.1164T>G	XP_011512069.1:p.Ile388Met
XM_011513768.1:c.1164T>G	XP_011512070.1:p.Ile388Met
XM_011513769.1:c.1284T>G	XP_011512071.1:p.Ile428Met
XM_011513770.1:c.888T>G	XP_011512072.1:p.Ile296Met
XM_011513771.1:c.888T>G	XP_011512073.1:p.Ile296Met
NM_001330751.1:c.1284T>G	NP_001317680.1:p.Ile428Met
NM_001330752.1:c.1233T>G	NP_001317681.1:p.Ile411Met
NM_001330753.1:c.888T>G	NP_001317682.1:p.Ile296Met
NM_001354825.1:c.1284T>G	NP_001341754.1:p.Ile428Met
NM_001354826.1:c.888T>G	NP_001341755.1:p.Ile296Met
NM_001354827.1:c.1284T>G	NP_001341756.1:p.Ile428Met
NM_013261.4:c.1269T>G	NP_037393.1:p.Ile423Met
NR_148981.1:n.1796T>G
NR_148982.1:n.1869T>G
NR_148983.1:n.2022T>G
NR_148984.1:n.1420T>G
NR_148985.1:n.1934T>G
NR_148986.1:n.1939T>G
NR_148987.1:n.2021T>G
XM_005248131.5:c.1281T>G	XP_005248188.1:p.Ile427Met
XM_005248134.4:c.1284T>G	XP_005248191.1:p.Ile428Met
XM_011513769.2:c.1284T>G	XP_011512071.1:p.Ile428Met
XM_024453878.1:c.1284T>G	XP_024309646.1:p.Ile428Met
NM_013261.5:c.1269T>G MANE Select	NP_037393.1:p.Ile423Met
NM_001330751.2:c.1284T>G	NP_001317680.1:p.Ile428Met
NM_001330752.2:c.1233T>G	NP_001317681.1:p.Ile411Met
NM_001354825.2:c.1284T>G	NP_001341754.1:p.Ile428Met
NM_001354826.2:c.888T>G	NP_001341755.1:p.Ile296Met
NM_001354827.2:c.1284T>G	NP_001341756.1:p.Ile428Met
NR_148981.2:n.1872T>G
NR_148982.2:n.1945T>G
NR_148983.2:n.2098T>G
NR_148984.2:n.1390T>G
NR_148985.2:n.2010T>G
NR_148986.2:n.2015T>G
NR_148987.2:n.2097T>G
NM_001330753.2:c.888T>G	NP_001317682.1:p.Ile296Met