Canonical Allele Identifier: CA374966223

Gene: FPGS

Linked Data

• MyVariant Identifiers: chr9:g.130575755A>T (hg19) ; chr9:g.127813476A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813476A>T , CM000671.2:g.127813476A>T	GRCh38
NC_000009.11:g.130575755A>T , CM000671.1:g.130575755A>T	GRCh37
NC_000009.10:g.129615576A>T	NCBI36
NG_009551.1:g.46293T>A , LRG_589:g.46293T>A
NG_023245.1:g.15602A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1636A>T MANE Select	ENSP00000362344.2:p.Thr546Ser
ENST00000373225.7:c.1486A>T	ENSP00000362322.3:p.Thr496Ser
ENST00000373247.6:c.1636A>T	ENSP00000362344.2:p.Thr546Ser
ENST00000393706.6:c.1558A>T	ENSP00000377309.2:p.Thr520Ser
ENST00000460181.5:n.1624A>T
ENST00000467826.5:n.709+153A>T
ENST00000475270.1:n.462A>T
ENST00000630236.2:c.*360A>T	ENSP00000486766.1:n.*360A>T
NM_001018078.2:c.1486A>T	NP_001018088.1:p.Thr496Ser
NM_001288803.1:c.1558A>T	NP_001275732.1:p.Thr520Ser
NM_004957.5:c.1636A>T	NP_004948.4:p.Thr546Ser
NR_110170.1:n.1684A>T
XM_005251864.2:c.1483+153A>T	XP_005251921.1:n.1483+153A>T
XM_011518437.1:c.1486A>T	XP_011516739.1:p.Thr496Ser
XM_011518438.1:c.1486A>T	XP_011516740.1:p.Thr496Ser
XM_011518439.1:c.793A>T	XP_011516741.1:p.Thr265Ser
XR_242581.2:n.1533A>T
XR_242582.2:n.1380+153A>T
XM_005251864.4:c.1483+153A>T	XP_005251921.1:n.1483+153A>T
XM_011518439.2:c.793A>T	XP_011516741.1:p.Thr265Ser
XM_017014565.2:c.1333+153A>T	XP_016870054.1:n.1333+153A>T
XM_017014566.1:c.793A>T	XP_016870055.1:p.Thr265Ser
XR_242581.4:n.1531A>T
XR_242582.4:n.1378+153A>T
NM_004957.6:c.1636A>T MANE Select	NP_004948.4:p.Thr546Ser