Canonical Allele Identifier: CA356524582

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815809A>C (hg19) ; chr4:g.23814186A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814186A>C , CM000666.2:g.23814186A>C	GRCh38
NC_000004.11:g.23815809A>C , CM000666.1:g.23815809A>C	GRCh37
NC_000004.10:g.23424907A>C	NCBI36
NG_028250.1:g.80892T>G
NG_028250.2:g.663790T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1297T>G MANE Select	ENSP00000264867.2:p.Tyr433Asp
ENST00000264867.6:c.1297T>G	ENSP00000264867.2:p.Tyr433Asp
ENST00000506055.5:c.*512T>G	ENSP00000423075.1:n.*512T>G
ENST00000509702.5:n.1337T>G
ENST00000613098.4:c.916T>G	ENSP00000481498.1:p.Tyr306Asp
NM_013261.3:c.1297T>G	NP_037393.1:p.Tyr433Asp
XM_005248130.2:c.1312T>G	XP_005248187.1:p.Tyr438Asp
XM_005248131.3:c.1309T>G	XP_005248188.1:p.Tyr437Asp
XM_005248132.1:c.1288T>G	XP_005248189.1:p.Tyr430Asp
XM_005248134.3:c.1312T>G	XP_005248191.1:p.Tyr438Asp
XM_011513764.1:c.1297T>G	XP_011512066.1:p.Tyr433Asp
XM_011513765.1:c.1261T>G	XP_011512067.1:p.Tyr421Asp
XM_011513766.1:c.1192T>G	XP_011512068.1:p.Tyr398Asp
XM_011513767.1:c.1192T>G	XP_011512069.1:p.Tyr398Asp
XM_011513768.1:c.1192T>G	XP_011512070.1:p.Tyr398Asp
XM_011513769.1:c.1312T>G	XP_011512071.1:p.Tyr438Asp
XM_011513770.1:c.916T>G	XP_011512072.1:p.Tyr306Asp
XM_011513771.1:c.916T>G	XP_011512073.1:p.Tyr306Asp
NM_001330751.1:c.1312T>G	NP_001317680.1:p.Tyr438Asp
NM_001330752.1:c.1261T>G	NP_001317681.1:p.Tyr421Asp
NM_001330753.1:c.916T>G	NP_001317682.1:p.Tyr306Asp
NM_001354825.1:c.1312T>G	NP_001341754.1:p.Tyr438Asp
NM_001354826.1:c.916T>G	NP_001341755.1:p.Tyr306Asp
NM_001354827.1:c.1312T>G	NP_001341756.1:p.Tyr438Asp
NM_013261.4:c.1297T>G	NP_037393.1:p.Tyr433Asp
NR_148981.1:n.1824T>G
NR_148982.1:n.1897T>G
NR_148983.1:n.2050T>G
NR_148984.1:n.1448T>G
NR_148985.1:n.1962T>G
NR_148986.1:n.1967T>G
NR_148987.1:n.2049T>G
XM_005248131.5:c.1309T>G	XP_005248188.1:p.Tyr437Asp
XM_005248134.4:c.1312T>G	XP_005248191.1:p.Tyr438Asp
XM_011513769.2:c.1312T>G	XP_011512071.1:p.Tyr438Asp
XM_024453878.1:c.1312T>G	XP_024309646.1:p.Tyr438Asp
NM_013261.5:c.1297T>G MANE Select	NP_037393.1:p.Tyr433Asp
NM_001330751.2:c.1312T>G	NP_001317680.1:p.Tyr438Asp
NM_001330752.2:c.1261T>G	NP_001317681.1:p.Tyr421Asp
NM_001354825.2:c.1312T>G	NP_001341754.1:p.Tyr438Asp
NM_001354826.2:c.916T>G	NP_001341755.1:p.Tyr306Asp
NM_001354827.2:c.1312T>G	NP_001341756.1:p.Tyr438Asp
NR_148981.2:n.1900T>G
NR_148982.2:n.1973T>G
NR_148983.2:n.2126T>G
NR_148984.2:n.1418T>G
NR_148985.2:n.2038T>G
NR_148986.2:n.2043T>G
NR_148987.2:n.2125T>G
NM_001330753.2:c.916T>G	NP_001317682.1:p.Tyr306Asp