Canonical Allele Identifier: CA438896069

Gene: PPARGC1A

Linked Data

• gnomAD v4: 4-23814067-A-G
• MyVariant Identifiers: chr4:g.23815690A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23814067A>G , CM000666.2:g.23814067A>G	GRCh38
NC_000004.11:g.23815690A>G , CM000666.1:g.23815690A>G	GRCh37
NC_000004.10:g.23424788A>G	NCBI36
NG_028250.1:g.81011T>C
NG_028250.2:g.663909T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1416T>C MANE Select	ENSP00000264867.2:p.Ala472=
ENST00000264867.6:c.1416T>C	ENSP00000264867.2:p.Ala472=
ENST00000506055.5:c.*631T>C	ENSP00000423075.1:n.*631T>C
ENST00000509702.5:n.1456T>C
ENST00000613098.4:c.1035T>C	ENSP00000481498.1:p.Ala345=
NM_013261.3:c.1416T>C	NP_037393.1:p.Ala472=
XM_005248130.2:c.1431T>C	XP_005248187.1:p.Ala477=
XM_005248131.3:c.1428T>C	XP_005248188.1:p.Ala476=
XM_005248132.1:c.1407T>C	XP_005248189.1:p.Ala469=
XM_005248134.3:c.1431T>C	XP_005248191.1:p.Ala477=
XM_011513764.1:c.1416T>C	XP_011512066.1:p.Ala472=
XM_011513765.1:c.1380T>C	XP_011512067.1:p.Ala460=
XM_011513766.1:c.1311T>C	XP_011512068.1:p.Ala437=
XM_011513767.1:c.1311T>C	XP_011512069.1:p.Ala437=
XM_011513768.1:c.1311T>C	XP_011512070.1:p.Ala437=
XM_011513769.1:c.1431T>C	XP_011512071.1:p.Ala477=
XM_011513770.1:c.1035T>C	XP_011512072.1:p.Ala345=
XM_011513771.1:c.1035T>C	XP_011512073.1:p.Ala345=
NM_001330751.1:c.1431T>C	NP_001317680.1:p.Ala477=
NM_001330752.1:c.1380T>C	NP_001317681.1:p.Ala460=
NM_001330753.1:c.1035T>C	NP_001317682.1:p.Ala345=
NM_001354825.1:c.1431T>C	NP_001341754.1:p.Ala477=
NM_001354826.1:c.1035T>C	NP_001341755.1:p.Ala345=
NM_001354827.1:c.1431T>C	NP_001341756.1:p.Ala477=
NM_013261.4:c.1416T>C	NP_037393.1:p.Ala472=
NR_148981.1:n.1943T>C
NR_148982.1:n.2016T>C
NR_148983.1:n.2169T>C
NR_148984.1:n.1567T>C
NR_148985.1:n.2081T>C
NR_148986.1:n.2086T>C
NR_148987.1:n.2168T>C
XM_005248131.5:c.1428T>C	XP_005248188.1:p.Ala476=
XM_005248134.4:c.1431T>C	XP_005248191.1:p.Ala477=
XM_011513769.2:c.1431T>C	XP_011512071.1:p.Ala477=
XM_024453878.1:c.1431T>C	XP_024309646.1:p.Ala477=
NM_013261.5:c.1416T>C MANE Select	NP_037393.1:p.Ala472=
NM_001330751.2:c.1431T>C	NP_001317680.1:p.Ala477=
NM_001330752.2:c.1380T>C	NP_001317681.1:p.Ala460=
NM_001354825.2:c.1431T>C	NP_001341754.1:p.Ala477=
NM_001354826.2:c.1035T>C	NP_001341755.1:p.Ala345=
NM_001354827.2:c.1431T>C	NP_001341756.1:p.Ala477=
NR_148981.2:n.2019T>C
NR_148982.2:n.2092T>C
NR_148983.2:n.2245T>C
NR_148984.2:n.1537T>C
NR_148985.2:n.2157T>C
NR_148986.2:n.2162T>C
NR_148987.2:n.2244T>C
NM_001330753.2:c.1035T>C	NP_001317682.1:p.Ala345=