Canonical Allele Identifier: CA2792929
Gene: PIGG HGNC NCBI

Linked Data

ClinVar Variation Id: 476325
ClinVar RCV Id: RCV000555697
dbSNP Id: rs34120878
gnomAD v2: 4-494194-C-G
gnomAD v3: 4-500405-C-G
gnomAD v4: 4-500405-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.500405C>G , CM000666.2:g.500405C>G GRCh38
NC_000004.11:g.494194C>G , CM000666.1:g.494194C>G GRCh37
NC_000004.10:g.484194C>G NCBI36
NG_051621.1:g.6206C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453061.7:c.164C>G MANE Select ENSP00000415203.2:p.Ser55Cys
ENST00000310340.9:c.164C>G ENSP00000311750.5:p.Ser55Cys
ENST00000383028.8:c.164C>G ENSP00000372494.4:p.Ser55Cys
ENST00000453061.6:c.164C>G ENSP00000415203.2:p.Ser55Cys
ENST00000502311.1:n.260C>G
ENST00000503111.5:c.-104C>G ENSP00000426002.1:n.-104C>G
ENST00000504187.5:c.164C>G ENSP00000427069.1:p.Ser55Cys
ENST00000504346.5:c.-104C>G ENSP00000424800.1:n.-104C>G
ENST00000506402.5:c.164C>G ENSP00000424619.1:p.Ser55Cys
ENST00000509768.1:c.-104C>G ENSP00000421550.1:n.-104C>G
ENST00000511448.5:c.164C>G ENSP00000423596.1:p.Ser55Cys
ENST00000514953.1:n.373-57C>G
NM_001127178.2:c.164C>G NP_001120650.1:p.Ser55Cys
NM_001289051.1:c.-104C>G NP_001275980.1:n.-104C>G
NM_001289052.1:c.164C>G NP_001275981.1:p.Ser55Cys
NM_001289053.1:c.-104C>G NP_001275982.1:n.-104C>G
NM_001289055.1:c.-273C>G NP_001275984.1:n.-273C>G
NM_001289057.1:c.-104C>G NP_001275986.1:n.-104C>G
NM_017733.4:c.164C>G NP_060203.3:p.Ser55Cys
NR_110293.1:n.300C>G
XM_005272283.2:c.164C>G XP_005272340.1:p.Ser55Cys
XM_005272284.2:c.-104C>G XP_005272341.1:n.-104C>G
XM_005272288.3:c.164C>G XP_005272345.1:p.Ser55Cys
XM_005272289.2:c.164C>G XP_005272346.1:p.Ser55Cys
XM_011513490.1:c.164C>G XP_011511792.1:p.Ser55Cys
XM_011513491.1:c.-273C>G XP_011511793.1:n.-273C>G
XM_011513493.1:c.164C>G XP_011511795.1:p.Ser55Cys
XM_011513494.1:c.164C>G XP_011511796.1:p.Ser55Cys
XR_924963.1:n.300C>G
XR_924965.1:n.300C>G
XR_924966.1:n.300C>G
XR_924967.1:n.300C>G
XR_924968.1:n.300C>G
XR_924969.1:n.300C>G
XR_924971.1:n.300C>G
XR_924972.1:n.300C>G
NM_001345986.1:c.-104C>G NP_001332915.1:n.-104C>G
NM_001345987.1:c.-104C>G NP_001332916.1:n.-104C>G
NM_001345988.1:c.-724C>G NP_001332917.1:n.-724C>G
NM_001345989.1:c.164C>G NP_001332918.1:p.Ser55Cys
NM_001345990.1:c.-1462C>G NP_001332919.1:n.-1462C>G
NM_001345991.1:c.-1324C>G NP_001332920.1:n.-1324C>G
NM_001345994.1:c.-1049C>G NP_001332923.1:n.-1049C>G
NR_144326.1:n.536C>G
NR_144327.1:n.300C>G
NR_144328.1:n.300C>G
NR_144329.1:n.536C>G
NR_144330.1:n.300C>G
NR_144331.1:n.536C>G
NR_144332.1:n.300C>G
NR_144333.1:n.300C>G
NR_144334.1:n.536C>G
XM_011513490.3:c.164C>G XP_011511792.1:p.Ser55Cys
XM_011513491.2:c.-273C>G XP_011511793.1:n.-273C>G
XM_011513494.3:c.164C>G XP_011511796.1:p.Ser55Cys
XR_001741248.2:n.276C>G
XR_001741251.2:n.276C>G
XR_001741253.2:n.276C>G
XR_001741254.2:n.276C>G
XR_001741255.2:n.276C>G
XR_001741258.2:n.276C>G
XR_001741259.2:n.276C>G
XR_001741261.2:n.276C>G
XR_001741262.2:n.276C>G
XR_002959736.1:n.276C>G
XR_002959737.1:n.276C>G
XR_002959738.1:n.276C>G
XR_924965.3:n.276C>G
XR_924967.3:n.276C>G
XR_924969.3:n.276C>G
XR_924972.3:n.276C>G
NM_001127178.3:c.164C>G MANE Select NP_001120650.1:p.Ser55Cys
NM_001345989.2:c.164C>G NP_001332918.1:p.Ser55Cys
NM_001289051.2:c.-104C>G NP_001275980.1:n.-104C>G
NM_001289052.2:c.164C>G NP_001275981.1:p.Ser55Cys
NM_001289053.2:c.-104C>G NP_001275982.1:n.-104C>G
NM_001289055.2:c.-273C>G NP_001275984.1:n.-273C>G
NM_001289057.2:c.-104C>G NP_001275986.1:n.-104C>G
NM_001345986.2:c.-104C>G NP_001332915.1:n.-104C>G
NM_001345987.2:c.-104C>G NP_001332916.1:n.-104C>G
NM_001345988.2:c.-724C>G NP_001332917.1:n.-724C>G
NM_001345990.2:c.-1462C>G NP_001332919.1:n.-1462C>G
NM_001345991.2:c.-1324C>G NP_001332920.1:n.-1324C>G
NM_001345994.2:c.-1049C>G NP_001332923.1:n.-1049C>G
NM_017733.5:c.164C>G NP_060203.3:p.Ser55Cys
NR_110293.2:n.290C>G
NR_144326.2:n.526C>G
NR_144327.2:n.290C>G
NR_144328.2:n.290C>G
NR_144329.2:n.526C>G
NR_144330.2:n.290C>G
NR_144331.2:n.526C>G
NR_144332.2:n.290C>G
NR_144333.2:n.290C>G
NR_144334.2:n.526C>G