Canonical Allele Identifier: CA1879977734

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813856_127813877delinsAGCCTGTCTCCCCCAACACCCC , CM000671.2:g.127813856_127813877delinsAGCCTGTCTCCCCCAACACCCC	GRCh38
NC_000009.11:g.130576135_130576156delinsAGCCTGTCTCCCCCAACACCCC , CM000671.1:g.130576135_130576156delinsAGCCTGTCTCCCCCAACACCCC	GRCh37
NC_000009.10:g.129615956_129615977delinsAGCCTGTCTCCCCCAACACCCC	NCBI36
NG_009551.1:g.45892_45913delinsGGGGTGTTGGGGGAGACAGGCT , LRG_589:g.45892_45913delinsGGGGTGTTGGGGGAGACAGGCT
NG_023245.1:g.15982_16003delinsAGCCTGTCTCCCCCAACACCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC MANE Select	ENSP00000362344.2:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
ENST00000373225.7:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	ENSP00000362322.3:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
ENST00000373247.6:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	ENSP00000362344.2:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
ENST00000393706.6:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	ENSP00000377309.2:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
ENST00000460181.5:n.2004_2025delinsAGCCTGTCTCCCCCAACACCCC
ENST00000467826.5:n.710-352_710-331delinsAGCCTGTCTCCCCCAACACCCC
ENST00000630236.2:c.*740_*761delinsAGCCTGTCTCCCCCAACACCCC	ENSP00000486766.1:n.*740_*761delinsAGCCTGTCTCCCCCAACACCCC
NM_001018078.2:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	NP_001018088.1:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
NM_001288803.1:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	NP_001275732.1:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
NM_004957.5:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	NP_004948.4:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
NR_110170.1:n.2064_2085delinsAGCCTGTCTCCCCCAACACCCC
XM_005251864.2:c.1484-352_1484-331delinsAGCCTGTCTCCCCCAACACCCC	XP_005251921.1:n.1484-352_1484-331delinsAGCCTGTCTCCCCCAACACCC...
XM_011518437.1:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	XP_011516739.1:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
XM_011518438.1:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	XP_011516740.1:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
XM_011518439.1:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	XP_011516741.1:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
XR_242581.2:n.1913_1934delinsAGCCTGTCTCCCCCAACACCCC
XR_242582.2:n.1381-352_1381-331delinsAGCCTGTCTCCCCCAACACCCC
XM_005251864.4:c.1484-352_1484-331delinsAGCCTGTCTCCCCCAACACCCC	XP_005251921.1:n.1484-352_1484-331delinsAGCCTGTCTCCCCCAACACCC...
XM_011518439.2:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	XP_011516741.1:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
XM_017014565.2:c.1334-352_1334-331delinsAGCCTGTCTCCCCCAACACCCC	XP_016870054.1:n.1334-352_1334-331delinsAGCCTGTCTCCCCCAACACCC...
XM_017014566.1:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC	XP_016870055.1:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC
XR_242581.4:n.1911_1932delinsAGCCTGTCTCCCCCAACACCCC
XR_242582.4:n.1379-352_1379-331delinsAGCCTGTCTCCCCCAACACCCC
NM_004957.6:c.*252_*273delinsAGCCTGTCTCCCCCAACACCCC MANE Select	NP_004948.4:n.*252_*273delinsAGCCTGTCTCCCCCAACACCCC