Canonical Allele Identifier: CA200297665

Gene: FPGS

Linked Data

• dbSNP Id: rs904142938
• gnomAD v2: 9-130576214-T-C
• gnomAD v3: 9-127813935-T-C
• gnomAD v4: 9-127813935-T-C
• MyVariant Identifiers: chr9:g.130576214T>C (hg19) ; chr9:g.127813935T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813935T>C , CM000671.2:g.127813935T>C	GRCh38
NC_000009.11:g.130576214T>C , CM000671.1:g.130576214T>C	GRCh37
NC_000009.10:g.129616035T>C	NCBI36
NG_009551.1:g.45834A>G , LRG_589:g.45834A>G
NG_023245.1:g.16061T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*331T>C MANE Select	ENSP00000362344.2:n.*331T>C
ENST00000373225.7:c.*331T>C	ENSP00000362322.3:n.*331T>C
ENST00000373247.6:c.*331T>C	ENSP00000362344.2:n.*331T>C
ENST00000393706.6:c.*331T>C	ENSP00000377309.2:n.*331T>C
ENST00000460181.5:n.2083T>C
ENST00000467826.5:n.710-273T>C
ENST00000630236.2:c.*819T>C	ENSP00000486766.1:n.*819T>C
NM_001018078.2:c.*331T>C	NP_001018088.1:n.*331T>C
NM_001288803.1:c.*331T>C	NP_001275732.1:n.*331T>C
NM_004957.5:c.*331T>C	NP_004948.4:n.*331T>C
NR_110170.1:n.2143T>C
XM_005251864.2:c.1484-273T>C	XP_005251921.1:n.1484-273T>C
XM_011518437.1:c.*331T>C	XP_011516739.1:n.*331T>C
XM_011518438.1:c.*331T>C	XP_011516740.1:n.*331T>C
XM_011518439.1:c.*331T>C	XP_011516741.1:n.*331T>C
XR_242581.2:n.1992T>C
XR_242582.2:n.1381-273T>C
XM_005251864.4:c.1484-273T>C	XP_005251921.1:n.1484-273T>C
XM_011518439.2:c.*331T>C	XP_011516741.1:n.*331T>C
XM_017014565.2:c.1334-273T>C	XP_016870054.1:n.1334-273T>C
XM_017014566.1:c.*331T>C	XP_016870055.1:n.*331T>C
XR_242581.4:n.1990T>C
XR_242582.4:n.1379-273T>C
NM_004957.6:c.*331T>C MANE Select	NP_004948.4:n.*331T>C