Canonical Allele Identifier: CA705220672

Gene: FAM177A1 PPP2R3C

Linked Data

• dbSNP Id: rs1362527206
• gnomAD v3: 14-35090102-CAG-C
• gnomAD v4: 14-35090102-CAG-C
• MyVariant Identifiers: chr14:g.35559309_35559310del (hg19) ; chr14:g.35090103_35090104del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35090103_35090104del , CM000676.2:g.35090103_35090104del	GRCh38
NC_000014.8:g.35559309_35559310del , CM000676.1:g.35559309_35559310del	GRCh37
NC_000014.7:g.34629060_34629061del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699514.1:c.*405-1991_*405-1990del (FAM177A1)	ENSP00000514409.1:n.*405-1991_*405-1990del
ENST00000699515.1:c.*332-1991_*332-1990del (FAM177A1)	ENSP00000514410.1:n.*332-1991_*332-1990del
ENST00000261475.10:c.1113+966_1113+967del (PPP2R3C) MANE Select	ENSP00000261475.5:n.1113+966_1113+967del
ENST00000261475.9:c.1113+966_1113+967del (PPP2R3C)	ENSP00000261475.5:n.1113+966_1113+967del
ENST00000553273.5:c.*779+966_*779+967del (PPP2R3C)	ENSP00000451075.1:n.*779+966_*779+967del
ENST00000554222.5:c.*916+966_*916+967del (PPP2R3C)	ENSP00000451416.1:n.*916+966_*916+967del
ENST00000555219.1:c.139-2094_139-2093del (PPP2R3C)	ENSP00000452173.1:n.139-2094_139-2093del
ENST00000555260.1:c.479+8544_479+8545del (FAM177A1)
ENST00000557074.1:c.110+966_110+967del (PPP2R3C)
ENST00000557217.5:c.*916+966_*916+967del (PPP2R3C)	ENSP00000452436.1:n.*916+966_*916+967del
NM_001305155.1:c.783+966_783+967del (PPP2R3C)	NP_001292084.1:n.783+966_783+967del
NM_001305156.1:c.783+966_783+967del (PPP2R3C)	NP_001292085.1:n.783+966_783+967del
NM_017917.2:c.1113+966_1113+967del (PPP2R3C)	NP_060387.2:n.1113+966_1113+967del
NM_017917.3:c.1113+966_1113+967del (PPP2R3C)	NP_060387.2:n.1113+966_1113+967del
NR_110415.1:n.479+8544_479+8545del
NR_130972.1:n.1312+966_1312+967del (PPP2R3C)
XM_005267782.2:c.1113+966_1113+967del (PPP2R3C)	XP_005267839.1:n.1113+966_1113+967del
XM_011536885.1:c.957+966_957+967del (PPP2R3C)	XP_011535187.1:n.957+966_957+967del
XM_005267782.4:c.1113+966_1113+967del (PPP2R3C)	XP_005267839.1:n.1113+966_1113+967del
XM_017021388.2:c.976-2094_976-2093del (PPP2R3C)	XP_016876877.1:n.976-2094_976-2093del
XM_024449638.1:c.1020+966_1020+967del (PPP2R3C)	XP_024305406.1:n.1020+966_1020+967del
XM_024449639.1:c.957+966_957+967del (PPP2R3C)	XP_024305407.1:n.957+966_957+967del
XR_002957558.1:n.1439+966_1439+967del (PPP2R3C)
NM_001305155.2:c.783+966_783+967del (PPP2R3C)	NP_001292084.1:n.783+966_783+967del
NM_001305156.2:c.783+966_783+967del (PPP2R3C)	NP_001292085.1:n.783+966_783+967del
NM_017917.4:c.1113+966_1113+967del (PPP2R3C) MANE Select	NP_060387.2:n.1113+966_1113+967del
NR_130972.2:n.1067+966_1067+967del (PPP2R3C)