Canonical Allele Identifier: CA467474170

Gene: FPGS

Linked Data

• MyVariant Identifiers: chr9:g.130575760C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813481C>T , CM000671.2:g.127813481C>T	GRCh38
NC_000009.11:g.130575760C>T , CM000671.1:g.130575760C>T	GRCh37
NC_000009.10:g.129615581C>T	NCBI36
NG_009551.1:g.46288G>A , LRG_589:g.46288G>A
NG_023245.1:g.15607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1641C>T MANE Select	ENSP00000362344.2:p.His547=
ENST00000373225.7:c.1491C>T	ENSP00000362322.3:p.His497=
ENST00000373247.6:c.1641C>T	ENSP00000362344.2:p.His547=
ENST00000393706.6:c.1563C>T	ENSP00000377309.2:p.His521=
ENST00000460181.5:n.1629C>T
ENST00000467826.5:n.709+158C>T
ENST00000475270.1:n.467C>T
ENST00000630236.2:c.*365C>T	ENSP00000486766.1:n.*365C>T
NM_001018078.2:c.1491C>T	NP_001018088.1:p.His497=
NM_001288803.1:c.1563C>T	NP_001275732.1:p.His521=
NM_004957.5:c.1641C>T	NP_004948.4:p.His547=
NR_110170.1:n.1689C>T
XM_005251864.2:c.1483+158C>T	XP_005251921.1:n.1483+158C>T
XM_011518437.1:c.1491C>T	XP_011516739.1:p.His497=
XM_011518438.1:c.1491C>T	XP_011516740.1:p.His497=
XM_011518439.1:c.798C>T	XP_011516741.1:p.His266=
XR_242581.2:n.1538C>T
XR_242582.2:n.1380+158C>T
XM_005251864.4:c.1483+158C>T	XP_005251921.1:n.1483+158C>T
XM_011518439.2:c.798C>T	XP_011516741.1:p.His266=
XM_017014565.2:c.1333+158C>T	XP_016870054.1:n.1333+158C>T
XM_017014566.1:c.798C>T	XP_016870055.1:p.His266=
XR_242581.4:n.1536C>T
XR_242582.4:n.1378+158C>T
NM_004957.6:c.1641C>T MANE Select	NP_004948.4:p.His547=