Canonical Allele Identifier: CA356524911

Gene: PPARGC1A

Linked Data

• MyVariant Identifiers: chr4:g.23815902G>A (hg19) ; chr4:g.23814279G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814279G>A , CM000666.2:g.23814279G>A	GRCh38
NC_000004.11:g.23815902G>A , CM000666.1:g.23815902G>A	GRCh37
NC_000004.10:g.23425000G>A	NCBI36
NG_028250.1:g.80799C>T
NG_028250.2:g.663697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1204C>T MANE Select	ENSP00000264867.2:p.Gln402Ter
ENST00000264867.6:c.1204C>T	ENSP00000264867.2:p.Gln402Ter
ENST00000506055.5:c.*419C>T	ENSP00000423075.1:n.*419C>T
ENST00000509702.5:n.1244C>T
ENST00000613098.4:c.823C>T	ENSP00000481498.1:p.Gln275Ter
NM_013261.3:c.1204C>T	NP_037393.1:p.Gln402Ter
XM_005248130.2:c.1219C>T	XP_005248187.1:p.Gln407Ter
XM_005248131.3:c.1216C>T	XP_005248188.1:p.Gln406Ter
XM_005248132.1:c.1195C>T	XP_005248189.1:p.Gln399Ter
XM_005248134.3:c.1219C>T	XP_005248191.1:p.Gln407Ter
XM_011513764.1:c.1204C>T	XP_011512066.1:p.Gln402Ter
XM_011513765.1:c.1168C>T	XP_011512067.1:p.Gln390Ter
XM_011513766.1:c.1099C>T	XP_011512068.1:p.Gln367Ter
XM_011513767.1:c.1099C>T	XP_011512069.1:p.Gln367Ter
XM_011513768.1:c.1099C>T	XP_011512070.1:p.Gln367Ter
XM_011513769.1:c.1219C>T	XP_011512071.1:p.Gln407Ter
XM_011513770.1:c.823C>T	XP_011512072.1:p.Gln275Ter
XM_011513771.1:c.823C>T	XP_011512073.1:p.Gln275Ter
NM_001330751.1:c.1219C>T	NP_001317680.1:p.Gln407Ter
NM_001330752.1:c.1168C>T	NP_001317681.1:p.Gln390Ter
NM_001330753.1:c.823C>T	NP_001317682.1:p.Gln275Ter
NM_001354825.1:c.1219C>T	NP_001341754.1:p.Gln407Ter
NM_001354826.1:c.823C>T	NP_001341755.1:p.Gln275Ter
NM_001354827.1:c.1219C>T	NP_001341756.1:p.Gln407Ter
NM_013261.4:c.1204C>T	NP_037393.1:p.Gln402Ter
NR_148981.1:n.1731C>T
NR_148982.1:n.1804C>T
NR_148983.1:n.1957C>T
NR_148984.1:n.1355C>T
NR_148985.1:n.1869C>T
NR_148986.1:n.1874C>T
NR_148987.1:n.1956C>T
XM_005248131.5:c.1216C>T	XP_005248188.1:p.Gln406Ter
XM_005248134.4:c.1219C>T	XP_005248191.1:p.Gln407Ter
XM_011513769.2:c.1219C>T	XP_011512071.1:p.Gln407Ter
XM_024453878.1:c.1219C>T	XP_024309646.1:p.Gln407Ter
NM_013261.5:c.1204C>T MANE Select	NP_037393.1:p.Gln402Ter
NM_001330751.2:c.1219C>T	NP_001317680.1:p.Gln407Ter
NM_001330752.2:c.1168C>T	NP_001317681.1:p.Gln390Ter
NM_001354825.2:c.1219C>T	NP_001341754.1:p.Gln407Ter
NM_001354826.2:c.823C>T	NP_001341755.1:p.Gln275Ter
NM_001354827.2:c.1219C>T	NP_001341756.1:p.Gln407Ter
NR_148981.2:n.1807C>T
NR_148982.2:n.1880C>T
NR_148983.2:n.2033C>T
NR_148984.2:n.1325C>T
NR_148985.2:n.1945C>T
NR_148986.2:n.1950C>T
NR_148987.2:n.2032C>T
NM_001330753.2:c.823C>T	NP_001317682.1:p.Gln275Ter