Canonical Allele Identifier: CA705220669

Gene: FAM177A1 PPP2R3C

Linked Data

• dbSNP Id: rs1363435244
• gnomAD v3: 14-35090097-TAC-T
• gnomAD v4: 14-35090097-TAC-T
• MyVariant Identifiers: chr14:g.35559304_35559305del (hg19) ; chr14:g.35090098_35090099del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35090098_35090099del , CM000676.2:g.35090098_35090099del	GRCh38
NC_000014.8:g.35559304_35559305del , CM000676.1:g.35559304_35559305del	GRCh37
NC_000014.7:g.34629055_34629056del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699514.1:c.*405-1996_*405-1995del (FAM177A1)	ENSP00000514409.1:n.*405-1996_*405-1995del
ENST00000699515.1:c.*332-1996_*332-1995del (FAM177A1)	ENSP00000514410.1:n.*332-1996_*332-1995del
ENST00000261475.10:c.1113+971_1113+972del (PPP2R3C) MANE Select	ENSP00000261475.5:n.1113+971_1113+972del
ENST00000261475.9:c.1113+971_1113+972del (PPP2R3C)	ENSP00000261475.5:n.1113+971_1113+972del
ENST00000553273.5:c.*779+971_*779+972del (PPP2R3C)	ENSP00000451075.1:n.*779+971_*779+972del
ENST00000554222.5:c.*916+971_*916+972del (PPP2R3C)	ENSP00000451416.1:n.*916+971_*916+972del
ENST00000555219.1:c.139-2089_139-2088del (PPP2R3C)	ENSP00000452173.1:n.139-2089_139-2088del
ENST00000555260.1:c.479+8539_479+8540del (FAM177A1)
ENST00000557074.1:c.110+971_110+972del (PPP2R3C)
ENST00000557217.5:c.*916+971_*916+972del (PPP2R3C)	ENSP00000452436.1:n.*916+971_*916+972del
NM_001305155.1:c.783+971_783+972del (PPP2R3C)	NP_001292084.1:n.783+971_783+972del
NM_001305156.1:c.783+971_783+972del (PPP2R3C)	NP_001292085.1:n.783+971_783+972del
NM_017917.2:c.1113+971_1113+972del (PPP2R3C)	NP_060387.2:n.1113+971_1113+972del
NM_017917.3:c.1113+971_1113+972del (PPP2R3C)	NP_060387.2:n.1113+971_1113+972del
NR_110415.1:n.479+8539_479+8540del
NR_130972.1:n.1312+971_1312+972del (PPP2R3C)
XM_005267782.2:c.1113+971_1113+972del (PPP2R3C)	XP_005267839.1:n.1113+971_1113+972del
XM_011536885.1:c.957+971_957+972del (PPP2R3C)	XP_011535187.1:n.957+971_957+972del
XM_005267782.4:c.1113+971_1113+972del (PPP2R3C)	XP_005267839.1:n.1113+971_1113+972del
XM_017021388.2:c.976-2089_976-2088del (PPP2R3C)	XP_016876877.1:n.976-2089_976-2088del
XM_024449638.1:c.1020+971_1020+972del (PPP2R3C)	XP_024305406.1:n.1020+971_1020+972del
XM_024449639.1:c.957+971_957+972del (PPP2R3C)	XP_024305407.1:n.957+971_957+972del
XR_002957558.1:n.1439+971_1439+972del (PPP2R3C)
NM_001305155.2:c.783+971_783+972del (PPP2R3C)	NP_001292084.1:n.783+971_783+972del
NM_001305156.2:c.783+971_783+972del (PPP2R3C)	NP_001292085.1:n.783+971_783+972del
NM_017917.4:c.1113+971_1113+972del (PPP2R3C) MANE Select	NP_060387.2:n.1113+971_1113+972del
NR_130972.2:n.1067+971_1067+972del (PPP2R3C)