Canonical Allele Identifier: CA1879977973

Gene: FPGS

Linked Data

• dbSNP Id: rs1830207853

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127814002C>T , CM000671.2:g.127814002C>T	GRCh38
NC_000009.11:g.130576281C>T , CM000671.1:g.130576281C>T	GRCh37
NC_000009.10:g.129616102C>T	NCBI36
NG_009551.1:g.45767G>A , LRG_589:g.45767G>A
NG_023245.1:g.16128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*398C>T MANE Select	ENSP00000362344.2:n.*398C>T
ENST00000373225.7:c.*398C>T	ENSP00000362322.3:n.*398C>T
ENST00000373247.6:c.*398C>T	ENSP00000362344.2:n.*398C>T
ENST00000393706.6:c.*398C>T	ENSP00000377309.2:n.*398C>T
ENST00000460181.5:n.2150C>T
ENST00000467826.5:n.710-206C>T
ENST00000630236.2:c.*886C>T	ENSP00000486766.1:n.*886C>T
NM_001018078.2:c.*398C>T	NP_001018088.1:n.*398C>T
NM_001288803.1:c.*398C>T	NP_001275732.1:n.*398C>T
NM_004957.5:c.*398C>T	NP_004948.4:n.*398C>T
NR_110170.1:n.2210C>T
XM_005251864.2:c.1484-206C>T	XP_005251921.1:n.1484-206C>T
XM_011518437.1:c.*398C>T	XP_011516739.1:n.*398C>T
XM_011518438.1:c.*398C>T	XP_011516740.1:n.*398C>T
XM_011518439.1:c.*398C>T	XP_011516741.1:n.*398C>T
XR_242581.2:n.2059C>T
XR_242582.2:n.1381-206C>T
XM_005251864.4:c.1484-206C>T	XP_005251921.1:n.1484-206C>T
XM_011518439.2:c.*398C>T	XP_011516741.1:n.*398C>T
XM_017014565.2:c.1334-206C>T	XP_016870054.1:n.1334-206C>T
XM_017014566.1:c.*398C>T	XP_016870055.1:n.*398C>T
XR_242581.4:n.2057C>T
XR_242582.4:n.1379-206C>T
NM_004957.6:c.*398C>T MANE Select	NP_004948.4:n.*398C>T