Canonical Allele Identifier: CA961881827

Gene: FAM177A1 PPP2R3C

Linked Data

• dbSNP Id: rs2045739817
• gnomAD v3: 14-35089859-G-GA
• gnomAD v4: 14-35089859-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35089859_35089860insA , CM000676.2:g.35089859_35089860insA	GRCh38
NC_000014.8:g.35559065_35559066insA , CM000676.1:g.35559065_35559066insA	GRCh37
NC_000014.7:g.34628816_34628817insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699514.1:c.*405-2235_*405-2234insA (FAM177A1)	ENSP00000514409.1:n.*405-2235_*405-2234insA
ENST00000699515.1:c.*332-2235_*332-2234insA (FAM177A1)	ENSP00000514410.1:n.*332-2235_*332-2234insA
ENST00000261475.10:c.1113+1210_1113+1211insT (PPP2R3C) MANE Select	ENSP00000261475.5:n.1113+1210_1113+1211insT
ENST00000261475.9:c.1113+1210_1113+1211insT (PPP2R3C)	ENSP00000261475.5:n.1113+1210_1113+1211insT
ENST00000553273.5:c.*779+1210_*779+1211insT (PPP2R3C)	ENSP00000451075.1:n.*779+1210_*779+1211insT
ENST00000554222.5:c.*916+1210_*916+1211insT (PPP2R3C)	ENSP00000451416.1:n.*916+1210_*916+1211insT
ENST00000555219.1:c.139-1850_139-1849insT (PPP2R3C)	ENSP00000452173.1:n.139-1850_139-1849insT
ENST00000555260.1:c.479+8300_479+8301insA (FAM177A1)
ENST00000557074.1:c.110+1210_110+1211insT (PPP2R3C)
ENST00000557217.5:c.*916+1210_*916+1211insT (PPP2R3C)	ENSP00000452436.1:n.*916+1210_*916+1211insT
NM_001305155.1:c.783+1210_783+1211insT (PPP2R3C)	NP_001292084.1:n.783+1210_783+1211insT
NM_001305156.1:c.783+1210_783+1211insT (PPP2R3C)	NP_001292085.1:n.783+1210_783+1211insT
NM_017917.2:c.1113+1210_1113+1211insT (PPP2R3C)	NP_060387.2:n.1113+1210_1113+1211insT
NM_017917.3:c.1113+1210_1113+1211insT (PPP2R3C)	NP_060387.2:n.1113+1210_1113+1211insT
NR_110415.1:n.479+8300_479+8301insA
NR_130972.1:n.1312+1210_1312+1211insT (PPP2R3C)
XM_005267782.2:c.1113+1210_1113+1211insT (PPP2R3C)	XP_005267839.1:n.1113+1210_1113+1211insT
XM_011536885.1:c.957+1210_957+1211insT (PPP2R3C)	XP_011535187.1:n.957+1210_957+1211insT
XM_005267782.4:c.1113+1210_1113+1211insT (PPP2R3C)	XP_005267839.1:n.1113+1210_1113+1211insT
XM_017021388.2:c.976-1850_976-1849insT (PPP2R3C)	XP_016876877.1:n.976-1850_976-1849insT
XM_024449638.1:c.1020+1210_1020+1211insT (PPP2R3C)	XP_024305406.1:n.1020+1210_1020+1211insT
XM_024449639.1:c.957+1210_957+1211insT (PPP2R3C)	XP_024305407.1:n.957+1210_957+1211insT
XR_002957558.1:n.1439+1210_1439+1211insT (PPP2R3C)
NM_001305155.2:c.783+1210_783+1211insT (PPP2R3C)	NP_001292084.1:n.783+1210_783+1211insT
NM_001305156.2:c.783+1210_783+1211insT (PPP2R3C)	NP_001292085.1:n.783+1210_783+1211insT
NM_017917.4:c.1113+1210_1113+1211insT (PPP2R3C) MANE Select	NP_060387.2:n.1113+1210_1113+1211insT
NR_130972.2:n.1067+1210_1067+1211insT (PPP2R3C)