Canonical Allele Identifier: CA1879977850

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813902_127813905delinsCTTA , CM000671.2:g.127813902_127813905delinsCTTA	GRCh38
NC_000009.11:g.130576181_130576184delinsCTTA , CM000671.1:g.130576181_130576184delinsCTTA	GRCh37
NC_000009.10:g.129616002_129616005delinsCTTA	NCBI36
NG_009551.1:g.45864_45867delinsTAAG , LRG_589:g.45864_45867delinsTAAG
NG_023245.1:g.16028_16031delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*298_*301delinsCTTA MANE Select	ENSP00000362344.2:n.*298_*301delinsCTTA
ENST00000373225.7:c.*298_*301delinsCTTA	ENSP00000362322.3:n.*298_*301delinsCTTA
ENST00000373247.6:c.*298_*301delinsCTTA	ENSP00000362344.2:n.*298_*301delinsCTTA
ENST00000393706.6:c.*298_*301delinsCTTA	ENSP00000377309.2:n.*298_*301delinsCTTA
ENST00000460181.5:n.2050_2053delinsCTTA
ENST00000467826.5:n.710-306_710-303delinsCTTA
ENST00000630236.2:c.*786_*789delinsCTTA	ENSP00000486766.1:n.*786_*789delinsCTTA
NM_001018078.2:c.*298_*301delinsCTTA	NP_001018088.1:n.*298_*301delinsCTTA
NM_001288803.1:c.*298_*301delinsCTTA	NP_001275732.1:n.*298_*301delinsCTTA
NM_004957.5:c.*298_*301delinsCTTA	NP_004948.4:n.*298_*301delinsCTTA
NR_110170.1:n.2110_2113delinsCTTA
XM_005251864.2:c.1484-306_1484-303delinsCTTA	XP_005251921.1:n.1484-306_1484-303delinsCTTA
XM_011518437.1:c.*298_*301delinsCTTA	XP_011516739.1:n.*298_*301delinsCTTA
XM_011518438.1:c.*298_*301delinsCTTA	XP_011516740.1:n.*298_*301delinsCTTA
XM_011518439.1:c.*298_*301delinsCTTA	XP_011516741.1:n.*298_*301delinsCTTA
XR_242581.2:n.1959_1962delinsCTTA
XR_242582.2:n.1381-306_1381-303delinsCTTA
XM_005251864.4:c.1484-306_1484-303delinsCTTA	XP_005251921.1:n.1484-306_1484-303delinsCTTA
XM_011518439.2:c.*298_*301delinsCTTA	XP_011516741.1:n.*298_*301delinsCTTA
XM_017014565.2:c.1334-306_1334-303delinsCTTA	XP_016870054.1:n.1334-306_1334-303delinsCTTA
XM_017014566.1:c.*298_*301delinsCTTA	XP_016870055.1:n.*298_*301delinsCTTA
XR_242581.4:n.1957_1960delinsCTTA
XR_242582.4:n.1379-306_1379-303delinsCTTA
NM_004957.6:c.*298_*301delinsCTTA MANE Select	NP_004948.4:n.*298_*301delinsCTTA