Canonical Allele Identifier: CA1444588755
Gene: PPARGC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.23853217_23853218delinsAG , CM000666.2:g.23853217_23853218delinsAG GRCh38
NC_000004.11:g.23854840_23854841delinsAG , CM000666.1:g.23854840_23854841delinsAG GRCh37
NC_000004.10:g.23463938_23463939delinsAG NCBI36
NG_028250.1:g.41860_41861delinsCT
NG_028250.2:g.624758_624759delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000264867.7:c.235-21467_235-21466delinsCT MANE Select ENSP00000264867.2:n.235-21467_235-21466de...
ENST00000264867.6:c.235-21467_235-21466delinsCT ENSP00000264867.2:n.235-21467_235-21466de...
ENST00000506055.5:c.235-21467_235-21466delinsCT ENSP00000423075.1:n.235-21467_235-21466de...
ENST00000507342.5:n.315-21467_315-21466delinsCT
ENST00000508380.1:n.155-21467_155-21466delinsCT
ENST00000509642.5:n.328-21467_328-21466delinsCT
ENST00000509702.5:n.192-21467_192-21466delinsCT
ENST00000512169.1:n.328-21467_328-21466delinsCT
ENST00000513205.5:c.235-21467_235-21466delinsCT ENSP00000421632.1:n.235-21467_235-21466de...
ENST00000612355.1:c.223-21467_223-21466delinsCT ENSP00000479729.1:n.223-21467_223-21466de...
ENST00000613098.4:c.-147-21467_-147-21466delinsCT ENSP00000481498.1:n.-147-21467_-147-21466...
ENST00000617484.4:c.223-21467_223-21466delinsCT ENSP00000477921.1:n.223-21467_223-21466de...
NM_013261.3:c.235-21467_235-21466delinsCT NP_037393.1:n.235-21467_235-21466delinsCT...
XM_005248130.2:c.250-21467_250-21466delinsCT XP_005248187.1:n.250-21467_250-21466delin...
XM_005248131.3:c.247-21467_247-21466delinsCT XP_005248188.1:n.247-21467_247-21466delin...
XM_005248132.1:c.226-21467_226-21466delinsCT XP_005248189.1:n.226-21467_226-21466delin...
XM_005248134.3:c.250-21467_250-21466delinsCT XP_005248191.1:n.250-21467_250-21466delin...
XM_011513764.1:c.235-21467_235-21466delinsCT XP_011512066.1:n.235-21467_235-21466delin...
XM_011513765.1:c.199-21467_199-21466delinsCT XP_011512067.1:n.199-21467_199-21466delin...
XM_011513766.1:c.130-21467_130-21466delinsCT XP_011512068.1:n.130-21467_130-21466delin...
XM_011513767.1:c.130-21467_130-21466delinsCT XP_011512069.1:n.130-21467_130-21466delin...
XM_011513768.1:c.130-21467_130-21466delinsCT XP_011512070.1:n.130-21467_130-21466delin...
XM_011513769.1:c.250-21467_250-21466delinsCT XP_011512071.1:n.250-21467_250-21466delin...
XM_011513770.1:c.-147-21467_-147-21466delinsCT XP_011512072.1:n.-147-21467_-147-21466del...
XM_011513771.1:c.-147-21467_-147-21466delinsCT XP_011512073.1:n.-147-21467_-147-21466del...
NM_001330751.1:c.250-21467_250-21466delinsCT NP_001317680.1:n.250-21467_250-21466delin...
NM_001330752.1:c.199-21467_199-21466delinsCT NP_001317681.1:n.199-21467_199-21466delin...
NM_001330753.1:c.-147-21467_-147-21466delinsCT NP_001317682.1:n.-147-21467_-147-21466del...
NM_001354825.1:c.250-21467_250-21466delinsCT NP_001341754.1:n.250-21467_250-21466delin...
NM_001354826.1:c.-147-21467_-147-21466delinsCT NP_001341755.1:n.-147-21467_-147-21466del...
NM_001354827.1:c.250-21467_250-21466delinsCT NP_001341756.1:n.250-21467_250-21466delin...
NM_013261.4:c.235-21467_235-21466delinsCT NP_037393.1:n.235-21467_235-21466delinsCT...
NR_148981.1:n.701-21467_701-21466delinsCT
NR_148982.1:n.804-21467_804-21466delinsCT
NR_148983.1:n.957-21467_957-21466delinsCT
NR_148984.1:n.355-21467_355-21466delinsCT
NR_148985.1:n.869-21467_869-21466delinsCT
NR_148986.1:n.701-21467_701-21466delinsCT
NR_148987.1:n.701-21467_701-21466delinsCT
XM_005248131.5:c.247-21467_247-21466delinsCT XP_005248188.1:n.247-21467_247-21466delin...
XM_005248134.4:c.250-21467_250-21466delinsCT XP_005248191.1:n.250-21467_250-21466delin...
XM_011513769.2:c.250-21467_250-21466delinsCT XP_011512071.1:n.250-21467_250-21466delin...
XM_024453878.1:c.250-21467_250-21466delinsCT XP_024309646.1:n.250-21467_250-21466delin...
NM_013261.5:c.235-21467_235-21466delinsCT MANE Select NP_037393.1:n.235-21467_235-21466delinsCT...
NM_001330751.2:c.250-21467_250-21466delinsCT NP_001317680.1:n.250-21467_250-21466delin...
NM_001330752.2:c.199-21467_199-21466delinsCT NP_001317681.1:n.199-21467_199-21466delin...
NM_001354825.2:c.250-21467_250-21466delinsCT NP_001341754.1:n.250-21467_250-21466delin...
NM_001354826.2:c.-147-21467_-147-21466delinsCT NP_001341755.1:n.-147-21467_-147-21466del...
NM_001354827.2:c.250-21467_250-21466delinsCT NP_001341756.1:n.250-21467_250-21466delin...
NR_148981.2:n.777-21467_777-21466delinsCT
NR_148982.2:n.880-21467_880-21466delinsCT
NR_148983.2:n.1033-21467_1033-21466delinsCT
NR_148984.2:n.325-21467_325-21466delinsCT
NR_148985.2:n.945-21467_945-21466delinsCT
NR_148986.2:n.777-21467_777-21466delinsCT
NR_148987.2:n.777-21467_777-21466delinsCT
NM_001330753.2:c.-147-21467_-147-21466delinsCT NP_001317682.1:n.-147-21467_-147-21466del...