Canonical Allele Identifier: CA2840908260

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813633del , CM000671.2:g.127813633del	GRCh38
NC_000009.11:g.130575912del , CM000671.1:g.130575912del	GRCh37
NC_000009.10:g.129615733del	NCBI36
NG_009551.1:g.46137del , LRG_589:g.46137del
NG_023245.1:g.15759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*29del MANE Select	ENSP00000362344.2:n.*29del
ENST00000373225.7:c.*29del	ENSP00000362322.3:n.*29del
ENST00000373247.6:c.*29del	ENSP00000362344.2:n.*29del
ENST00000393706.6:c.*29del	ENSP00000377309.2:n.*29del
ENST00000460181.5:n.1781del
ENST00000467826.5:n.709+310del
ENST00000630236.2:c.*517del	ENSP00000486766.1:n.*517del
NM_001018078.2:c.*29del	NP_001018088.1:n.*29del
NM_001288803.1:c.*29del	NP_001275732.1:n.*29del
NM_004957.5:c.*29del	NP_004948.4:n.*29del
NR_110170.1:n.1841del
XM_005251864.2:c.1483+310del	XP_005251921.1:n.1483+310del
XM_011518437.1:c.*29del	XP_011516739.1:n.*29del
XM_011518438.1:c.*29del	XP_011516740.1:n.*29del
XM_011518439.1:c.*29del	XP_011516741.1:n.*29del
XR_242581.2:n.1690del
XR_242582.2:n.1380+310del
XM_005251864.4:c.1483+310del	XP_005251921.1:n.1483+310del
XM_011518439.2:c.*29del	XP_011516741.1:n.*29del
XM_017014565.2:c.1333+310del	XP_016870054.1:n.1333+310del
XM_017014566.1:c.*29del	XP_016870055.1:n.*29del
XR_242581.4:n.1688del
XR_242582.4:n.1378+310del
NM_004957.6:c.*29del MANE Select	NP_004948.4:n.*29del