Canonical Allele Identifier: CA2793107
Community Standard Title: NM_001127178.3(PIGG):c.771G>A (p.Thr257=)
Gene: PIGG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.508840G>A , CM000666.2:g.508840G>A GRCh38
NC_000004.11:g.502629G>A , CM000666.1:g.502629G>A GRCh37
NC_000004.10:g.492629G>A NCBI36
NG_051621.1:g.14641G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001127178.3:c.771G>A MANE Select NP_001120650.1:p.Thr257=
ENST00000453061.7:c.771G>A MANE Select ENSP00000415203.2:p.Thr257=
NM_001127178.2:c.771G>A NP_001120650.1:p.Thr257=
NM_001289051.1:c.504G>A NP_001275980.1:p.Thr168=
NM_001289051.2:c.504G>A NP_001275980.1:p.Thr168=
NM_001289052.1:c.372G>A NP_001275981.1:p.Thr124=
NM_001289052.2:c.372G>A NP_001275981.1:p.Thr124=
NM_001289053.1:c.504G>A NP_001275982.1:p.Thr168=
NM_001289053.2:c.504G>A NP_001275982.1:p.Thr168=
NM_001289055.1:c.405G>A NP_001275984.1:p.Thr135=
NM_001289055.2:c.405G>A NP_001275984.1:p.Thr135=
NM_001289057.1:c.504G>A NP_001275986.1:p.Thr168=
NM_001289057.2:c.504G>A NP_001275986.1:p.Thr168=
NM_001345986.1:c.504G>A NP_001332915.1:p.Thr168=
NM_001345986.2:c.504G>A NP_001332915.1:p.Thr168=
NM_001345987.1:c.504G>A NP_001332916.1:p.Thr168=
NM_001345987.2:c.504G>A NP_001332916.1:p.Thr168=
NM_001345988.1:c.-129+1247G>A NP_001332917.1:n.-129+1247G>A
NM_001345988.2:c.-129+1247G>A NP_001332917.1:n.-129+1247G>A
NM_001345989.1:c.771G>A NP_001332918.1:p.Thr257=
NM_001345989.2:c.771G>A NP_001332918.1:p.Thr257=
NM_001345990.1:c.-855G>A NP_001332919.1:n.-855G>A
NM_001345990.2:c.-855G>A NP_001332919.1:n.-855G>A
NM_001345991.1:c.-717G>A NP_001332920.1:n.-717G>A
NM_001345991.2:c.-717G>A NP_001332920.1:n.-717G>A
NM_001345994.1:c.-442G>A NP_001332923.1:n.-442G>A
NM_001345994.2:c.-442G>A NP_001332923.1:n.-442G>A
NM_017733.4:c.771G>A NP_060203.3:p.Thr257=
NM_017733.5:c.771G>A NP_060203.3:p.Thr257=
NR_110293.1:n.907G>A
NR_110293.2:n.897G>A
NR_144326.1:n.1143G>A
NR_144326.2:n.1133G>A
NR_144327.1:n.907G>A
NR_144327.2:n.897G>A
NR_144328.1:n.907G>A
NR_144328.2:n.897G>A
NR_144329.1:n.1143G>A
NR_144329.2:n.1133G>A
NR_144330.1:n.907G>A
NR_144330.2:n.897G>A
NR_144331.1:n.1143G>A
NR_144331.2:n.1133G>A
NR_144332.1:n.907G>A
NR_144332.2:n.897G>A
NR_144333.1:n.907G>A
NR_144333.2:n.897G>A
NR_144334.1:n.1143G>A
NR_144334.2:n.1133G>A
ENST00000310340.9:c.771G>A ENSP00000311750.5:p.Thr257=
ENST00000383028.8:c.372G>A ENSP00000372494.4:p.Thr124=
ENST00000453061.6:c.771G>A ENSP00000415203.2:p.Thr257=
ENST00000503111.5:c.504G>A ENSP00000426002.1:p.Thr168=
ENST00000504187.5:c.*280G>A ENSP00000427069.1:n.*280G>A
ENST00000504346.5:c.504G>A ENSP00000424800.1:p.Thr168=
ENST00000506402.5:c.771G>A ENSP00000424619.1:p.Thr257=
ENST00000509768.1:c.504G>A ENSP00000421550.1:p.Thr168=
XM_005272283.2:c.561G>A XP_005272340.1:p.Thr187=
XM_005272284.2:c.504G>A XP_005272341.1:p.Thr168=
XM_005272288.3:c.771G>A XP_005272345.1:p.Thr257=
XM_005272289.2:c.771G>A XP_005272346.1:p.Thr257=
XM_011513490.1:c.771G>A XP_011511792.1:p.Thr257=
XM_011513490.3:c.771G>A XP_011511792.1:p.Thr257=
XM_011513491.1:c.405G>A XP_011511793.1:p.Thr135=
XM_011513491.2:c.405G>A XP_011511793.1:p.Thr135=
XM_011513493.1:c.771G>A XP_011511795.1:p.Thr257=
XM_011513494.1:c.771G>A XP_011511796.1:p.Thr257=
XM_011513494.3:c.771G>A XP_011511796.1:p.Thr257=
XR_001741248.2:n.883G>A
XR_001741251.2:n.883G>A
XR_001741253.2:n.883G>A
XR_001741254.2:n.883G>A
XR_001741255.2:n.883G>A
XR_001741258.2:n.883G>A
XR_001741259.2:n.883G>A
XR_001741261.2:n.883G>A
XR_001741262.2:n.883G>A
XR_002959736.1:n.883G>A
XR_002959737.1:n.883G>A
XR_002959738.1:n.883G>A
XR_924963.1:n.907G>A
XR_924965.1:n.907G>A
XR_924965.3:n.883G>A
XR_924966.1:n.907G>A
XR_924967.1:n.907G>A
XR_924967.3:n.883G>A
XR_924968.1:n.907G>A
XR_924969.1:n.907G>A
XR_924969.3:n.883G>A
XR_924971.1:n.907G>A
XR_924972.1:n.907G>A
XR_924972.3:n.883G>A