Canonical Allele Identifier: CA961881613

Gene: FAM177A1 PPP2R3C

Linked Data

• gnomAD v3: 14-35089765-A-AAG
• gnomAD v4: 14-35089765-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35089765_35089766insAG , CM000676.2:g.35089765_35089766insAG	GRCh38
NC_000014.8:g.35558971_35558972insAG , CM000676.1:g.35558971_35558972insAG	GRCh37
NC_000014.7:g.34628722_34628723insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699514.1:c.*405-2329_*405-2328insAG (FAM177A1)	ENSP00000514409.1:n.*405-2329_*405-2328insAG
ENST00000699515.1:c.*332-2329_*332-2328insAG (FAM177A1)	ENSP00000514410.1:n.*332-2329_*332-2328insAG
ENST00000261475.10:c.1113+1304_1113+1305insCT (PPP2R3C) MANE Select	ENSP00000261475.5:n.1113+1304_1113+1305insCT
ENST00000261475.9:c.1113+1304_1113+1305insCT (PPP2R3C)	ENSP00000261475.5:n.1113+1304_1113+1305insCT
ENST00000553273.5:c.*779+1304_*779+1305insCT (PPP2R3C)	ENSP00000451075.1:n.*779+1304_*779+1305insCT
ENST00000554222.5:c.*916+1304_*916+1305insCT (PPP2R3C)	ENSP00000451416.1:n.*916+1304_*916+1305insCT
ENST00000555219.1:c.139-1756_139-1755insCT (PPP2R3C)	ENSP00000452173.1:n.139-1756_139-1755insCT
ENST00000555260.1:c.479+8206_479+8207insAG (FAM177A1)
ENST00000557074.1:c.110+1304_110+1305insCT (PPP2R3C)
ENST00000557217.5:c.*916+1304_*916+1305insCT (PPP2R3C)	ENSP00000452436.1:n.*916+1304_*916+1305insCT
NM_001305155.1:c.783+1304_783+1305insCT (PPP2R3C)	NP_001292084.1:n.783+1304_783+1305insCT
NM_001305156.1:c.783+1304_783+1305insCT (PPP2R3C)	NP_001292085.1:n.783+1304_783+1305insCT
NM_017917.2:c.1113+1304_1113+1305insCT (PPP2R3C)	NP_060387.2:n.1113+1304_1113+1305insCT
NM_017917.3:c.1113+1304_1113+1305insCT (PPP2R3C)	NP_060387.2:n.1113+1304_1113+1305insCT
NR_110415.1:n.479+8206_479+8207insAG
NR_130972.1:n.1312+1304_1312+1305insCT (PPP2R3C)
XM_005267782.2:c.1113+1304_1113+1305insCT (PPP2R3C)	XP_005267839.1:n.1113+1304_1113+1305insCT
XM_011536885.1:c.957+1304_957+1305insCT (PPP2R3C)	XP_011535187.1:n.957+1304_957+1305insCT
XM_005267782.4:c.1113+1304_1113+1305insCT (PPP2R3C)	XP_005267839.1:n.1113+1304_1113+1305insCT
XM_017021388.2:c.976-1756_976-1755insCT (PPP2R3C)	XP_016876877.1:n.976-1756_976-1755insCT
XM_024449638.1:c.1020+1304_1020+1305insCT (PPP2R3C)	XP_024305406.1:n.1020+1304_1020+1305insCT
XM_024449639.1:c.957+1304_957+1305insCT (PPP2R3C)	XP_024305407.1:n.957+1304_957+1305insCT
XR_002957558.1:n.1439+1304_1439+1305insCT (PPP2R3C)
NM_001305155.2:c.783+1304_783+1305insCT (PPP2R3C)	NP_001292084.1:n.783+1304_783+1305insCT
NM_001305156.2:c.783+1304_783+1305insCT (PPP2R3C)	NP_001292085.1:n.783+1304_783+1305insCT
NM_017917.4:c.1113+1304_1113+1305insCT (PPP2R3C) MANE Select	NP_060387.2:n.1113+1304_1113+1305insCT
NR_130972.2:n.1067+1304_1067+1305insCT (PPP2R3C)