Canonical Allele Identifier: CA2497374158

Gene: FAM177A1 PPP2R3C

Linked Data

• dbSNP Id: rs2045739334

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35089856_35089857insA , CM000676.2:g.35089856_35089857insA	GRCh38
NC_000014.8:g.35559062_35559063insA , CM000676.1:g.35559062_35559063insA	GRCh37
NC_000014.7:g.34628813_34628814insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699514.1:c.*405-2238_*405-2237insA (FAM177A1)	ENSP00000514409.1:n.*405-2238_*405-2237insA
ENST00000699515.1:c.*332-2238_*332-2237insA (FAM177A1)	ENSP00000514410.1:n.*332-2238_*332-2237insA
ENST00000261475.10:c.1113+1213_1113+1214insT (PPP2R3C) MANE Select	ENSP00000261475.5:n.1113+1213_1113+1214insT
ENST00000261475.9:c.1113+1213_1113+1214insT (PPP2R3C)	ENSP00000261475.5:n.1113+1213_1113+1214insT
ENST00000553273.5:c.*779+1213_*779+1214insT (PPP2R3C)	ENSP00000451075.1:n.*779+1213_*779+1214insT
ENST00000554222.5:c.*916+1213_*916+1214insT (PPP2R3C)	ENSP00000451416.1:n.*916+1213_*916+1214insT
ENST00000555219.1:c.139-1847_139-1846insT (PPP2R3C)	ENSP00000452173.1:n.139-1847_139-1846insT
ENST00000555260.1:c.479+8297_479+8298insA (FAM177A1)
ENST00000557074.1:c.110+1213_110+1214insT (PPP2R3C)
ENST00000557217.5:c.*916+1213_*916+1214insT (PPP2R3C)	ENSP00000452436.1:n.*916+1213_*916+1214insT
NM_001305155.1:c.783+1213_783+1214insT (PPP2R3C)	NP_001292084.1:n.783+1213_783+1214insT
NM_001305156.1:c.783+1213_783+1214insT (PPP2R3C)	NP_001292085.1:n.783+1213_783+1214insT
NM_017917.2:c.1113+1213_1113+1214insT (PPP2R3C)	NP_060387.2:n.1113+1213_1113+1214insT
NM_017917.3:c.1113+1213_1113+1214insT (PPP2R3C)	NP_060387.2:n.1113+1213_1113+1214insT
NR_110415.1:n.479+8297_479+8298insA
NR_130972.1:n.1312+1213_1312+1214insT (PPP2R3C)
XM_005267782.2:c.1113+1213_1113+1214insT (PPP2R3C)	XP_005267839.1:n.1113+1213_1113+1214insT
XM_011536885.1:c.957+1213_957+1214insT (PPP2R3C)	XP_011535187.1:n.957+1213_957+1214insT
XM_005267782.4:c.1113+1213_1113+1214insT (PPP2R3C)	XP_005267839.1:n.1113+1213_1113+1214insT
XM_017021388.2:c.976-1847_976-1846insT (PPP2R3C)	XP_016876877.1:n.976-1847_976-1846insT
XM_024449638.1:c.1020+1213_1020+1214insT (PPP2R3C)	XP_024305406.1:n.1020+1213_1020+1214insT
XM_024449639.1:c.957+1213_957+1214insT (PPP2R3C)	XP_024305407.1:n.957+1213_957+1214insT
XR_002957558.1:n.1439+1213_1439+1214insT (PPP2R3C)
NM_001305155.2:c.783+1213_783+1214insT (PPP2R3C)	NP_001292084.1:n.783+1213_783+1214insT
NM_001305156.2:c.783+1213_783+1214insT (PPP2R3C)	NP_001292085.1:n.783+1213_783+1214insT
NM_017917.4:c.1113+1213_1113+1214insT (PPP2R3C) MANE Select	NP_060387.2:n.1113+1213_1113+1214insT
NR_130972.2:n.1067+1213_1067+1214insT (PPP2R3C)