Canonical Allele Identifier: CA1444632081
Gene: PPARGC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23814062A= , CM000666.2:g.23814062A= GRCh38
NC_000004.11:g.23815685A= , CM000666.1:g.23815685A= GRCh37
NC_000004.10:g.23424783A= NCBI36
NG_028250.1:g.81016T=
NG_028250.2:g.663914T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264867.7:c.1421T= MANE Select ENSP00000264867.2:p.Phe474=
ENST00000264867.6:c.1421T= ENSP00000264867.2:p.Phe474=
ENST00000506055.5:c.*636T= ENSP00000423075.1:n.*636T=
ENST00000509702.5:n.1461T=
ENST00000613098.4:c.1040T= ENSP00000481498.1:p.Phe347=
NM_013261.3:c.1421T= NP_037393.1:p.Phe474=
XM_005248130.2:c.1436T= XP_005248187.1:p.Phe479=
XM_005248131.3:c.1433T= XP_005248188.1:p.Phe478=
XM_005248132.1:c.1412T= XP_005248189.1:p.Phe471=
XM_005248134.3:c.1436T= XP_005248191.1:p.Phe479=
XM_011513764.1:c.1421T= XP_011512066.1:p.Phe474=
XM_011513765.1:c.1385T= XP_011512067.1:p.Phe462=
XM_011513766.1:c.1316T= XP_011512068.1:p.Phe439=
XM_011513767.1:c.1316T= XP_011512069.1:p.Phe439=
XM_011513768.1:c.1316T= XP_011512070.1:p.Phe439=
XM_011513769.1:c.1436T= XP_011512071.1:p.Phe479=
XM_011513770.1:c.1040T= XP_011512072.1:p.Phe347=
XM_011513771.1:c.1040T= XP_011512073.1:p.Phe347=
NM_001330751.1:c.1436T= NP_001317680.1:p.Phe479=
NM_001330752.1:c.1385T= NP_001317681.1:p.Phe462=
NM_001330753.1:c.1040T= NP_001317682.1:p.Phe347=
NM_001354825.1:c.1436T= NP_001341754.1:p.Phe479=
NM_001354826.1:c.1040T= NP_001341755.1:p.Phe347=
NM_001354827.1:c.1436T= NP_001341756.1:p.Phe479=
NM_013261.4:c.1421T= NP_037393.1:p.Phe474=
NR_148981.1:n.1948T=
NR_148982.1:n.2021T=
NR_148983.1:n.2174T=
NR_148984.1:n.1572T=
NR_148985.1:n.2086T=
NR_148986.1:n.2091T=
NR_148987.1:n.2173T=
XM_005248131.5:c.1433T= XP_005248188.1:p.Phe478=
XM_005248134.4:c.1436T= XP_005248191.1:p.Phe479=
XM_011513769.2:c.1436T= XP_011512071.1:p.Phe479=
XM_024453878.1:c.1436T= XP_024309646.1:p.Phe479=
NM_013261.5:c.1421T= MANE Select NP_037393.1:p.Phe474=
NM_001330751.2:c.1436T= NP_001317680.1:p.Phe479=
NM_001330752.2:c.1385T= NP_001317681.1:p.Phe462=
NM_001354825.2:c.1436T= NP_001341754.1:p.Phe479=
NM_001354826.2:c.1040T= NP_001341755.1:p.Phe347=
NM_001354827.2:c.1436T= NP_001341756.1:p.Phe479=
NR_148981.2:n.2024T=
NR_148982.2:n.2097T=
NR_148983.2:n.2250T=
NR_148984.2:n.1542T=
NR_148985.2:n.2162T=
NR_148986.2:n.2167T=
NR_148987.2:n.2249T=
NM_001330753.2:c.1040T= NP_001317682.1:p.Phe347=