Canonical Allele Identifier: CA356524084

Gene: PPARGC1A

Linked Data

• dbSNP Id: rs1721443056
• gnomAD v4: 4-23813966-G-A
• MyVariant Identifiers: chr4:g.23815589G>A (hg19) ; chr4:g.23813966G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.23813966G>A , CM000666.2:g.23813966G>A	GRCh38
NC_000004.11:g.23815589G>A , CM000666.1:g.23815589G>A	GRCh37
NC_000004.10:g.23424687G>A	NCBI36
NG_028250.1:g.81112C>T
NG_028250.2:g.664010C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264867.7:c.1517C>T MANE Select	ENSP00000264867.2:p.Ala506Val
ENST00000264867.6:c.1517C>T	ENSP00000264867.2:p.Ala506Val
ENST00000506055.5:c.*732C>T	ENSP00000423075.1:n.*732C>T
ENST00000509702.5:n.1557C>T
ENST00000613098.4:c.1136C>T	ENSP00000481498.1:p.Ala379Val
NM_013261.3:c.1517C>T	NP_037393.1:p.Ala506Val
XM_005248130.2:c.1532C>T	XP_005248187.1:p.Ala511Val
XM_005248131.3:c.1529C>T	XP_005248188.1:p.Ala510Val
XM_005248132.1:c.1508C>T	XP_005248189.1:p.Ala503Val
XM_005248134.3:c.1532C>T	XP_005248191.1:p.Ala511Val
XM_011513764.1:c.1517C>T	XP_011512066.1:p.Ala506Val
XM_011513765.1:c.1481C>T	XP_011512067.1:p.Ala494Val
XM_011513766.1:c.1412C>T	XP_011512068.1:p.Ala471Val
XM_011513767.1:c.1412C>T	XP_011512069.1:p.Ala471Val
XM_011513768.1:c.1412C>T	XP_011512070.1:p.Ala471Val
XM_011513769.1:c.1532C>T	XP_011512071.1:p.Ala511Val
XM_011513770.1:c.1136C>T	XP_011512072.1:p.Ala379Val
XM_011513771.1:c.1136C>T	XP_011512073.1:p.Ala379Val
NM_001330751.1:c.1532C>T	NP_001317680.1:p.Ala511Val
NM_001330752.1:c.1481C>T	NP_001317681.1:p.Ala494Val
NM_001330753.1:c.1136C>T	NP_001317682.1:p.Ala379Val
NM_001354825.1:c.1532C>T	NP_001341754.1:p.Ala511Val
NM_001354826.1:c.1136C>T	NP_001341755.1:p.Ala379Val
NM_001354827.1:c.1532C>T	NP_001341756.1:p.Ala511Val
NM_013261.4:c.1517C>T	NP_037393.1:p.Ala506Val
NR_148981.1:n.2044C>T
NR_148982.1:n.2117C>T
NR_148983.1:n.2270C>T
NR_148984.1:n.1668C>T
NR_148985.1:n.2182C>T
NR_148986.1:n.2187C>T
NR_148987.1:n.2269C>T
XM_005248131.5:c.1529C>T	XP_005248188.1:p.Ala510Val
XM_005248134.4:c.1532C>T	XP_005248191.1:p.Ala511Val
XM_011513769.2:c.1532C>T	XP_011512071.1:p.Ala511Val
XM_024453878.1:c.1532C>T	XP_024309646.1:p.Ala511Val
NM_013261.5:c.1517C>T MANE Select	NP_037393.1:p.Ala506Val
NM_001330751.2:c.1532C>T	NP_001317680.1:p.Ala511Val
NM_001330752.2:c.1481C>T	NP_001317681.1:p.Ala494Val
NM_001354825.2:c.1532C>T	NP_001341754.1:p.Ala511Val
NM_001354826.2:c.1136C>T	NP_001341755.1:p.Ala379Val
NM_001354827.2:c.1532C>T	NP_001341756.1:p.Ala511Val
NR_148981.2:n.2120C>T
NR_148982.2:n.2193C>T
NR_148983.2:n.2346C>T
NR_148984.2:n.1638C>T
NR_148985.2:n.2258C>T
NR_148986.2:n.2263C>T
NR_148987.2:n.2345C>T
NM_001330753.2:c.1136C>T	NP_001317682.1:p.Ala379Val