Canonical Allele Identifier: CA91066569
Community Standard Title: NM_001127178.3(PIGG):c.1615-106T>C
Gene: PIGG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.523353T>C , CM000666.2:g.523353T>C GRCh38
NC_000004.11:g.517142T>C , CM000666.1:g.517142T>C GRCh37
NC_000004.10:g.507142T>C NCBI36
NG_051621.1:g.29154T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001127178.3:c.1615-106T>C MANE Select NP_001120650.1:n.1615-106T>C
ENST00000453061.7:c.1615-106T>C MANE Select ENSP00000415203.2:n.1615-106T>C
NM_001127178.2:c.1615-106T>C NP_001120650.1:n.1615-106T>C
NM_001289051.1:c.1348-106T>C NP_001275980.1:n.1348-106T>C
NM_001289051.2:c.1348-106T>C NP_001275980.1:n.1348-106T>C
NM_001289052.1:c.1216-106T>C NP_001275981.1:n.1216-106T>C
NM_001289052.2:c.1216-106T>C NP_001275981.1:n.1216-106T>C
NM_001345986.1:c.1348-106T>C NP_001332915.1:n.1348-106T>C
NM_001345986.2:c.1348-106T>C NP_001332915.1:n.1348-106T>C
NM_001345987.1:c.1324-106T>C NP_001332916.1:n.1324-106T>C
NM_001345987.2:c.1324-106T>C NP_001332916.1:n.1324-106T>C
NM_001345988.1:c.586-106T>C NP_001332917.1:n.586-106T>C
NM_001345988.2:c.586-106T>C NP_001332917.1:n.586-106T>C
NM_001345990.1:c.82-106T>C NP_001332919.1:n.82-106T>C
NM_001345990.2:c.82-106T>C NP_001332919.1:n.82-106T>C
NM_001345991.1:c.82-106T>C NP_001332920.1:n.82-106T>C
NM_001345991.2:c.82-106T>C NP_001332920.1:n.82-106T>C
NM_001345994.1:c.517-106T>C NP_001332923.1:n.517-106T>C
NM_001345994.2:c.517-106T>C NP_001332923.1:n.517-106T>C
NM_017733.4:c.1591-106T>C NP_060203.3:n.1591-106T>C
NM_017733.5:c.1591-106T>C NP_060203.3:n.1591-106T>C
NR_110293.1:n.1705-106T>C
NR_110293.2:n.1695-106T>C
NR_144326.1:n.1987-106T>C
NR_144326.2:n.1977-106T>C
NR_144327.1:n.1751-106T>C
NR_144327.2:n.1741-106T>C
NR_144328.1:n.2174-106T>C
NR_144328.2:n.2164-106T>C
NR_144329.1:n.1941-106T>C
NR_144329.2:n.1931-106T>C
NR_144330.1:n.1751-106T>C
NR_144330.2:n.1741-106T>C
NR_144331.1:n.1987-106T>C
NR_144331.2:n.1977-106T>C
NR_144332.1:n.1750+1412T>C
NR_144332.2:n.1740+1412T>C
NR_144333.1:n.1750+1412T>C
NR_144333.2:n.1740+1412T>C
NR_144334.1:n.1940+1412T>C
NR_144334.2:n.1930+1412T>C
ENST00000310340.9:c.1591-106T>C ENSP00000311750.5:n.1591-106T>C
ENST00000383028.8:c.1216-106T>C ENSP00000372494.4:n.1216-106T>C
ENST00000453061.6:c.1615-106T>C ENSP00000415203.2:n.1615-106T>C
ENST00000504346.5:c.1348-106T>C ENSP00000424800.1:n.1348-106T>C
ENST00000508562.1:n.53-106T>C
XM_005272283.2:c.1405-106T>C XP_005272340.1:n.1405-106T>C
XM_005272284.2:c.1348-106T>C XP_005272341.1:n.1348-106T>C
XM_005272288.3:c.1615-106T>C XP_005272345.1:n.1615-106T>C
XM_005272289.2:c.1614+1412T>C XP_005272346.1:n.1614+1412T>C
XM_011513490.1:c.1615-106T>C XP_011511792.1:n.1615-106T>C
XM_011513490.3:c.1615-106T>C XP_011511792.1:n.1615-106T>C
XM_011513491.1:c.1249-106T>C XP_011511793.1:n.1249-106T>C
XM_011513491.2:c.1249-106T>C XP_011511793.1:n.1249-106T>C
XM_011513492.1:c.541-106T>C XP_011511794.1:n.541-106T>C
XR_001741248.2:n.1727-106T>C
XR_001741251.2:n.1727-106T>C
XR_001741253.2:n.1727-106T>C
XR_001741254.2:n.1727-106T>C
XR_001741255.2:n.1727-106T>C
XR_001741258.2:n.1755+1412T>C
XR_001741259.2:n.1756-106T>C
XR_001741261.2:n.1680+1412T>C
XR_001741262.2:n.1841-106T>C
XR_002959736.1:n.1727-106T>C
XR_002959737.1:n.3167T>C
XR_002959738.1:n.3092T>C
XR_924963.1:n.1751-106T>C
XR_924965.1:n.1751-106T>C
XR_924965.3:n.1727-106T>C
XR_924966.1:n.1751-106T>C
XR_924967.1:n.1751-106T>C
XR_924967.3:n.1727-106T>C
XR_924968.1:n.1751-106T>C
XR_924969.1:n.1751-106T>C
XR_924969.3:n.1727-106T>C
XR_924971.1:n.1751-106T>C
XR_924972.1:n.1751-106T>C
XR_924972.3:n.1727-106T>C