Canonical Allele Identifier: CA356524552

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815794A>C (hg19) ; chr4:g.23814171A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814171A>C , CM000666.2:g.23814171A>C	GRCh38
NC_000004.11:g.23815794A>C , CM000666.1:g.23815794A>C	GRCh37
NC_000004.10:g.23424892A>C	NCBI36
NG_028250.1:g.80907T>G
NG_028250.2:g.663805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1312T>G MANE Select	ENSP00000264867.2:p.Leu438Val
ENST00000264867.6:c.1312T>G	ENSP00000264867.2:p.Leu438Val
ENST00000506055.5:c.*527T>G	ENSP00000423075.1:n.*527T>G
ENST00000509702.5:n.1352T>G
ENST00000613098.4:c.931T>G	ENSP00000481498.1:p.Leu311Val
NM_013261.3:c.1312T>G	NP_037393.1:p.Leu438Val
XM_005248130.2:c.1327T>G	XP_005248187.1:p.Leu443Val
XM_005248131.3:c.1324T>G	XP_005248188.1:p.Leu442Val
XM_005248132.1:c.1303T>G	XP_005248189.1:p.Leu435Val
XM_005248134.3:c.1327T>G	XP_005248191.1:p.Leu443Val
XM_011513764.1:c.1312T>G	XP_011512066.1:p.Leu438Val
XM_011513765.1:c.1276T>G	XP_011512067.1:p.Leu426Val
XM_011513766.1:c.1207T>G	XP_011512068.1:p.Leu403Val
XM_011513767.1:c.1207T>G	XP_011512069.1:p.Leu403Val
XM_011513768.1:c.1207T>G	XP_011512070.1:p.Leu403Val
XM_011513769.1:c.1327T>G	XP_011512071.1:p.Leu443Val
XM_011513770.1:c.931T>G	XP_011512072.1:p.Leu311Val
XM_011513771.1:c.931T>G	XP_011512073.1:p.Leu311Val
NM_001330751.1:c.1327T>G	NP_001317680.1:p.Leu443Val
NM_001330752.1:c.1276T>G	NP_001317681.1:p.Leu426Val
NM_001330753.1:c.931T>G	NP_001317682.1:p.Leu311Val
NM_001354825.1:c.1327T>G	NP_001341754.1:p.Leu443Val
NM_001354826.1:c.931T>G	NP_001341755.1:p.Leu311Val
NM_001354827.1:c.1327T>G	NP_001341756.1:p.Leu443Val
NM_013261.4:c.1312T>G	NP_037393.1:p.Leu438Val
NR_148981.1:n.1839T>G
NR_148982.1:n.1912T>G
NR_148983.1:n.2065T>G
NR_148984.1:n.1463T>G
NR_148985.1:n.1977T>G
NR_148986.1:n.1982T>G
NR_148987.1:n.2064T>G
XM_005248131.5:c.1324T>G	XP_005248188.1:p.Leu442Val
XM_005248134.4:c.1327T>G	XP_005248191.1:p.Leu443Val
XM_011513769.2:c.1327T>G	XP_011512071.1:p.Leu443Val
XM_024453878.1:c.1327T>G	XP_024309646.1:p.Leu443Val
NM_013261.5:c.1312T>G MANE Select	NP_037393.1:p.Leu438Val
NM_001330751.2:c.1327T>G	NP_001317680.1:p.Leu443Val
NM_001330752.2:c.1276T>G	NP_001317681.1:p.Leu426Val
NM_001354825.2:c.1327T>G	NP_001341754.1:p.Leu443Val
NM_001354826.2:c.931T>G	NP_001341755.1:p.Leu311Val
NM_001354827.2:c.1327T>G	NP_001341756.1:p.Leu443Val
NR_148981.2:n.1915T>G
NR_148982.2:n.1988T>G
NR_148983.2:n.2141T>G
NR_148984.2:n.1433T>G
NR_148985.2:n.2053T>G
NR_148986.2:n.2058T>G
NR_148987.2:n.2140T>G
NM_001330753.2:c.931T>G	NP_001317682.1:p.Leu311Val