Canonical Allele Identifier: CA2793465
Community Standard Title: NM_001127178.3(PIGG):c.1854C>T (p.Ala618=)
Gene: PIGG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.523698C>T , CM000666.2:g.523698C>T GRCh38
NC_000004.11:g.517487C>T , CM000666.1:g.517487C>T GRCh37
NC_000004.10:g.507487C>T NCBI36
NG_051621.1:g.29499C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001127178.3:c.1854C>T MANE Select NP_001120650.1:p.Ala618=
ENST00000453061.7:c.1854C>T MANE Select ENSP00000415203.2:p.Ala618=
NM_001127178.2:c.1854C>T NP_001120650.1:p.Ala618=
NM_001289051.1:c.1587C>T NP_001275980.1:p.Ala529=
NM_001289051.2:c.1587C>T NP_001275980.1:p.Ala529=
NM_001289052.1:c.1455C>T NP_001275981.1:p.Ala485=
NM_001289052.2:c.1455C>T NP_001275981.1:p.Ala485=
NM_001345986.1:c.1587C>T NP_001332915.1:p.Ala529=
NM_001345986.2:c.1587C>T NP_001332915.1:p.Ala529=
NM_001345987.1:c.1563C>T NP_001332916.1:p.Ala521=
NM_001345987.2:c.1563C>T NP_001332916.1:p.Ala521=
NM_001345988.1:c.825C>T NP_001332917.1:p.Ala275=
NM_001345988.2:c.825C>T NP_001332917.1:p.Ala275=
NM_001345990.1:c.321C>T NP_001332919.1:p.Ala107=
NM_001345990.2:c.321C>T NP_001332919.1:p.Ala107=
NM_001345991.1:c.321C>T NP_001332920.1:p.Ala107=
NM_001345991.2:c.321C>T NP_001332920.1:p.Ala107=
NM_001345994.1:c.756C>T NP_001332923.1:p.Ala252=
NM_001345994.2:c.756C>T NP_001332923.1:p.Ala252=
NM_017733.4:c.1830C>T NP_060203.3:p.Ala610=
NM_017733.5:c.1830C>T NP_060203.3:p.Ala610=
NR_110293.1:n.1944C>T
NR_110293.2:n.1934C>T
NR_144326.1:n.2226C>T
NR_144326.2:n.2216C>T
NR_144327.1:n.1990C>T
NR_144327.2:n.1980C>T
NR_144328.1:n.2413C>T
NR_144328.2:n.2403C>T
NR_144329.1:n.2133+47C>T
NR_144329.2:n.2123+47C>T
NR_144330.1:n.1990C>T
NR_144330.2:n.1980C>T
NR_144331.1:n.2226C>T
NR_144331.2:n.2216C>T
NR_144332.1:n.1750+1757C>T
NR_144332.2:n.1740+1757C>T
NR_144333.1:n.1750+1757C>T
NR_144333.2:n.1740+1757C>T
NR_144334.1:n.1940+1757C>T
NR_144334.2:n.1930+1757C>T
ENST00000310340.9:c.1830C>T ENSP00000311750.5:p.Ala610=
ENST00000383028.8:c.1455C>T ENSP00000372494.4:p.Ala485=
ENST00000453061.6:c.1854C>T ENSP00000415203.2:p.Ala618=
ENST00000504346.5:c.1587C>T ENSP00000424800.1:p.Ala529=
ENST00000508562.1:n.292C>T
ENST00000511247.1:n.179C>T
XM_005272283.2:c.1644C>T XP_005272340.1:p.Ala548=
XM_005272284.2:c.1587C>T XP_005272341.1:p.Ala529=
XM_005272288.3:c.1807+47C>T XP_005272345.1:n.1807+47C>T
XM_005272289.2:c.1614+1757C>T XP_005272346.1:n.1614+1757C>T
XM_011513490.1:c.1854C>T XP_011511792.1:p.Ala618=
XM_011513490.3:c.1854C>T XP_011511792.1:p.Ala618=
XM_011513491.1:c.1488C>T XP_011511793.1:p.Ala496=
XM_011513491.2:c.1488C>T XP_011511793.1:p.Ala496=
XM_011513492.1:c.780C>T XP_011511794.1:p.Ala260=
XR_001741248.2:n.1966C>T
XR_001741251.2:n.1966C>T
XR_001741253.2:n.1919+47C>T
XR_001741254.2:n.1919+47C>T
XR_001741255.2:n.1919+47C>T
XR_001741258.2:n.1755+1757C>T
XR_001741259.2:n.1995C>T
XR_001741261.2:n.1680+1757C>T
XR_001741262.2:n.2033+47C>T
XR_002959736.1:n.1966C>T
XR_002959737.1:n.3512C>T
XR_002959738.1:n.3437C>T
XR_924963.1:n.1990C>T
XR_924965.1:n.1990C>T
XR_924965.3:n.1966C>T
XR_924966.1:n.1990C>T
XR_924967.1:n.1990C>T
XR_924967.3:n.1966C>T
XR_924968.1:n.1990C>T
XR_924969.1:n.1990C>T
XR_924969.3:n.1966C>T
XR_924971.1:n.1943+47C>T
XR_924972.1:n.1943+47C>T
XR_924972.3:n.1919+47C>T