Canonical Allele Identifier: CA2691804019

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813771-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813771T>C , CM000671.2:g.127813771T>C	GRCh38
NC_000009.11:g.130576050T>C , CM000671.1:g.130576050T>C	GRCh37
NC_000009.10:g.129615871T>C	NCBI36
NG_009551.1:g.45998A>G , LRG_589:g.45998A>G
NG_023245.1:g.15897T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*167T>C MANE Select	ENSP00000362344.2:n.*167T>C
ENST00000373225.7:c.*167T>C	ENSP00000362322.3:n.*167T>C
ENST00000373247.6:c.*167T>C	ENSP00000362344.2:n.*167T>C
ENST00000393706.6:c.*167T>C	ENSP00000377309.2:n.*167T>C
ENST00000460181.5:n.1919T>C
ENST00000467826.5:n.710-437T>C
ENST00000630236.2:c.*655T>C	ENSP00000486766.1:n.*655T>C
NM_001018078.2:c.*167T>C	NP_001018088.1:n.*167T>C
NM_001288803.1:c.*167T>C	NP_001275732.1:n.*167T>C
NM_004957.5:c.*167T>C	NP_004948.4:n.*167T>C
NR_110170.1:n.1979T>C
XM_005251864.2:c.1484-437T>C	XP_005251921.1:n.1484-437T>C
XM_011518437.1:c.*167T>C	XP_011516739.1:n.*167T>C
XM_011518438.1:c.*167T>C	XP_011516740.1:n.*167T>C
XM_011518439.1:c.*167T>C	XP_011516741.1:n.*167T>C
XR_242581.2:n.1828T>C
XR_242582.2:n.1381-437T>C
XM_005251864.4:c.1484-437T>C	XP_005251921.1:n.1484-437T>C
XM_011518439.2:c.*167T>C	XP_011516741.1:n.*167T>C
XM_017014565.2:c.1334-437T>C	XP_016870054.1:n.1334-437T>C
XM_017014566.1:c.*167T>C	XP_016870055.1:n.*167T>C
XR_242581.4:n.1826T>C
XR_242582.4:n.1379-437T>C
NM_004957.6:c.*167T>C MANE Select	NP_004948.4:n.*167T>C