Canonical Allele Identifier: CA1879977450

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813624_127813645delinsGTGGGAGCTTCCCACACCTGCC , CM000671.2:g.127813624_127813645delinsGTGGGAGCTTCCCACACCTGCC	GRCh38
NC_000009.11:g.130575903_130575924delinsGTGGGAGCTTCCCACACCTGCC , CM000671.1:g.130575903_130575924delinsGTGGGAGCTTCCCACACCTGCC	GRCh37
NC_000009.10:g.129615724_129615745delinsGTGGGAGCTTCCCACACCTGCC	NCBI36
NG_009551.1:g.46124_46145delinsGGCAGGTGTGGGAAGCTCCCAC , LRG_589:g.46124_46145delinsGGCAGGTGTGGGAAGCTCCCAC
NG_023245.1:g.15750_15771delinsGTGGGAGCTTCCCACACCTGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC MANE Select	ENSP00000362344.2:n.*20_*41delinsGTGGGAGC...
ENST00000373225.7:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	ENSP00000362322.3:n.*20_*41delinsGTGGGAGC...
ENST00000373247.6:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	ENSP00000362344.2:n.*20_*41delinsGTGGGAGC...
ENST00000393706.6:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	ENSP00000377309.2:n.*20_*41delinsGTGGGAGC...
ENST00000460181.5:n.1772_1793delinsGTGGGAGCTTCCCACACCTGCC
ENST00000467826.5:n.709+301_709+322delinsGTGGGAGCTTCCCACACCTGCC
ENST00000630236.2:c.*508_*529delinsGTGGGAGCTTCCCACACCTGCC	ENSP00000486766.1:n.*508_*529delinsGTGGGA...
NM_001018078.2:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	NP_001018088.1:n.*20_*41delinsGTGGGAGCTTC...
NM_001288803.1:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	NP_001275732.1:n.*20_*41delinsGTGGGAGCTTC...
NM_004957.5:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	NP_004948.4:n.*20_*41delinsGTGGGAGCTTCCCA...
NR_110170.1:n.1832_1853delinsGTGGGAGCTTCCCACACCTGCC
XM_005251864.2:c.1483+301_1483+322delinsGTGGGAGCTTCCCACACCTGCC	XP_005251921.1:n.1483+301_1483+322delinsG...
XM_011518437.1:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	XP_011516739.1:n.*20_*41delinsGTGGGAGCTTC...
XM_011518438.1:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	XP_011516740.1:n.*20_*41delinsGTGGGAGCTTC...
XM_011518439.1:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	XP_011516741.1:n.*20_*41delinsGTGGGAGCTTC...
XR_242581.2:n.1681_1702delinsGTGGGAGCTTCCCACACCTGCC
XR_242582.2:n.1380+301_1380+322delinsGTGGGAGCTTCCCACACCTGCC
XM_005251864.4:c.1483+301_1483+322delinsGTGGGAGCTTCCCACACCTGCC	XP_005251921.1:n.1483+301_1483+322delinsG...
XM_011518439.2:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	XP_011516741.1:n.*20_*41delinsGTGGGAGCTTC...
XM_017014565.2:c.1333+301_1333+322delinsGTGGGAGCTTCCCACACCTGCC	XP_016870054.1:n.1333+301_1333+322delinsG...
XM_017014566.1:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC	XP_016870055.1:n.*20_*41delinsGTGGGAGCTTC...
XR_242581.4:n.1679_1700delinsGTGGGAGCTTCCCACACCTGCC
XR_242582.4:n.1378+301_1378+322delinsGTGGGAGCTTCCCACACCTGCC
NM_004957.6:c.*20_*41delinsGTGGGAGCTTCCCACACCTGCC MANE Select	NP_004948.4:n.*20_*41delinsGTGGGAGCTTCCCA...