Canonical Allele Identifier: CA356524466

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815756T>A (hg19) ; chr4:g.23814133T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814133T>A , CM000666.2:g.23814133T>A	GRCh38
NC_000004.11:g.23815756T>A , CM000666.1:g.23815756T>A	GRCh37
NC_000004.10:g.23424854T>A	NCBI36
NG_028250.1:g.80945A>T
NG_028250.2:g.663843A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1350A>T MANE Select	ENSP00000264867.2:p.Arg450Ser
ENST00000264867.6:c.1350A>T	ENSP00000264867.2:p.Arg450Ser
ENST00000506055.5:c.*565A>T	ENSP00000423075.1:n.*565A>T
ENST00000509702.5:n.1390A>T
ENST00000613098.4:c.969A>T	ENSP00000481498.1:p.Arg323Ser
NM_013261.3:c.1350A>T	NP_037393.1:p.Arg450Ser
XM_005248130.2:c.1365A>T	XP_005248187.1:p.Arg455Ser
XM_005248131.3:c.1362A>T	XP_005248188.1:p.Arg454Ser
XM_005248132.1:c.1341A>T	XP_005248189.1:p.Arg447Ser
XM_005248134.3:c.1365A>T	XP_005248191.1:p.Arg455Ser
XM_011513764.1:c.1350A>T	XP_011512066.1:p.Arg450Ser
XM_011513765.1:c.1314A>T	XP_011512067.1:p.Arg438Ser
XM_011513766.1:c.1245A>T	XP_011512068.1:p.Arg415Ser
XM_011513767.1:c.1245A>T	XP_011512069.1:p.Arg415Ser
XM_011513768.1:c.1245A>T	XP_011512070.1:p.Arg415Ser
XM_011513769.1:c.1365A>T	XP_011512071.1:p.Arg455Ser
XM_011513770.1:c.969A>T	XP_011512072.1:p.Arg323Ser
XM_011513771.1:c.969A>T	XP_011512073.1:p.Arg323Ser
NM_001330751.1:c.1365A>T	NP_001317680.1:p.Arg455Ser
NM_001330752.1:c.1314A>T	NP_001317681.1:p.Arg438Ser
NM_001330753.1:c.969A>T	NP_001317682.1:p.Arg323Ser
NM_001354825.1:c.1365A>T	NP_001341754.1:p.Arg455Ser
NM_001354826.1:c.969A>T	NP_001341755.1:p.Arg323Ser
NM_001354827.1:c.1365A>T	NP_001341756.1:p.Arg455Ser
NM_013261.4:c.1350A>T	NP_037393.1:p.Arg450Ser
NR_148981.1:n.1877A>T
NR_148982.1:n.1950A>T
NR_148983.1:n.2103A>T
NR_148984.1:n.1501A>T
NR_148985.1:n.2015A>T
NR_148986.1:n.2020A>T
NR_148987.1:n.2102A>T
XM_005248131.5:c.1362A>T	XP_005248188.1:p.Arg454Ser
XM_005248134.4:c.1365A>T	XP_005248191.1:p.Arg455Ser
XM_011513769.2:c.1365A>T	XP_011512071.1:p.Arg455Ser
XM_024453878.1:c.1365A>T	XP_024309646.1:p.Arg455Ser
NM_013261.5:c.1350A>T MANE Select	NP_037393.1:p.Arg450Ser
NM_001330751.2:c.1365A>T	NP_001317680.1:p.Arg455Ser
NM_001330752.2:c.1314A>T	NP_001317681.1:p.Arg438Ser
NM_001354825.2:c.1365A>T	NP_001341754.1:p.Arg455Ser
NM_001354826.2:c.969A>T	NP_001341755.1:p.Arg323Ser
NM_001354827.2:c.1365A>T	NP_001341756.1:p.Arg455Ser
NR_148981.2:n.1953A>T
NR_148982.2:n.2026A>T
NR_148983.2:n.2179A>T
NR_148984.2:n.1471A>T
NR_148985.2:n.2091A>T
NR_148986.2:n.2096A>T
NR_148987.2:n.2178A>T
NM_001330753.2:c.969A>T	NP_001317682.1:p.Arg323Ser