Canonical Allele Identifier: CA438896096

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815738C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814115C>T , CM000666.2:g.23814115C>T	GRCh38
NC_000004.11:g.23815738C>T , CM000666.1:g.23815738C>T	GRCh37
NC_000004.10:g.23424836C>T	NCBI36
NG_028250.1:g.80963G>A
NG_028250.2:g.663861G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1368G>A MANE Select	ENSP00000264867.2:p.Gln456=
ENST00000264867.6:c.1368G>A	ENSP00000264867.2:p.Gln456=
ENST00000506055.5:c.*583G>A	ENSP00000423075.1:n.*583G>A
ENST00000509702.5:n.1408G>A
ENST00000613098.4:c.987G>A	ENSP00000481498.1:p.Gln329=
NM_013261.3:c.1368G>A	NP_037393.1:p.Gln456=
XM_005248130.2:c.1383G>A	XP_005248187.1:p.Gln461=
XM_005248131.3:c.1380G>A	XP_005248188.1:p.Gln460=
XM_005248132.1:c.1359G>A	XP_005248189.1:p.Gln453=
XM_005248134.3:c.1383G>A	XP_005248191.1:p.Gln461=
XM_011513764.1:c.1368G>A	XP_011512066.1:p.Gln456=
XM_011513765.1:c.1332G>A	XP_011512067.1:p.Gln444=
XM_011513766.1:c.1263G>A	XP_011512068.1:p.Gln421=
XM_011513767.1:c.1263G>A	XP_011512069.1:p.Gln421=
XM_011513768.1:c.1263G>A	XP_011512070.1:p.Gln421=
XM_011513769.1:c.1383G>A	XP_011512071.1:p.Gln461=
XM_011513770.1:c.987G>A	XP_011512072.1:p.Gln329=
XM_011513771.1:c.987G>A	XP_011512073.1:p.Gln329=
NM_001330751.1:c.1383G>A	NP_001317680.1:p.Gln461=
NM_001330752.1:c.1332G>A	NP_001317681.1:p.Gln444=
NM_001330753.1:c.987G>A	NP_001317682.1:p.Gln329=
NM_001354825.1:c.1383G>A	NP_001341754.1:p.Gln461=
NM_001354826.1:c.987G>A	NP_001341755.1:p.Gln329=
NM_001354827.1:c.1383G>A	NP_001341756.1:p.Gln461=
NM_013261.4:c.1368G>A	NP_037393.1:p.Gln456=
NR_148981.1:n.1895G>A
NR_148982.1:n.1968G>A
NR_148983.1:n.2121G>A
NR_148984.1:n.1519G>A
NR_148985.1:n.2033G>A
NR_148986.1:n.2038G>A
NR_148987.1:n.2120G>A
XM_005248131.5:c.1380G>A	XP_005248188.1:p.Gln460=
XM_005248134.4:c.1383G>A	XP_005248191.1:p.Gln461=
XM_011513769.2:c.1383G>A	XP_011512071.1:p.Gln461=
XM_024453878.1:c.1383G>A	XP_024309646.1:p.Gln461=
NM_013261.5:c.1368G>A MANE Select	NP_037393.1:p.Gln456=
NM_001330751.2:c.1383G>A	NP_001317680.1:p.Gln461=
NM_001330752.2:c.1332G>A	NP_001317681.1:p.Gln444=
NM_001354825.2:c.1383G>A	NP_001341754.1:p.Gln461=
NM_001354826.2:c.987G>A	NP_001341755.1:p.Gln329=
NM_001354827.2:c.1383G>A	NP_001341756.1:p.Gln461=
NR_148981.2:n.1971G>A
NR_148982.2:n.2044G>A
NR_148983.2:n.2197G>A
NR_148984.2:n.1489G>A
NR_148985.2:n.2109G>A
NR_148986.2:n.2114G>A
NR_148987.2:n.2196G>A
NM_001330753.2:c.987G>A	NP_001317682.1:p.Gln329=