Canonical Allele Identifier: CA374966526

Gene: FPGS

Linked Data

• MyVariant Identifiers: chr9:g.130575779G>T (hg19) ; chr9:g.127813500G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813500G>T , CM000671.2:g.127813500G>T	GRCh38
NC_000009.11:g.130575779G>T , CM000671.1:g.130575779G>T	GRCh37
NC_000009.10:g.129615600G>T	NCBI36
NG_009551.1:g.46269C>A , LRG_589:g.46269C>A
NG_023245.1:g.15626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1660G>T MANE Select	ENSP00000362344.2:p.Ala554Ser
ENST00000373225.7:c.1510G>T	ENSP00000362322.3:p.Ala504Ser
ENST00000373247.6:c.1660G>T	ENSP00000362344.2:p.Ala554Ser
ENST00000393706.6:c.1582G>T	ENSP00000377309.2:p.Ala528Ser
ENST00000460181.5:n.1648G>T
ENST00000467826.5:n.709+177G>T
ENST00000475270.1:n.486G>T
ENST00000630236.2:c.*384G>T	ENSP00000486766.1:n.*384G>T
NM_001018078.2:c.1510G>T	NP_001018088.1:p.Ala504Ser
NM_001288803.1:c.1582G>T	NP_001275732.1:p.Ala528Ser
NM_004957.5:c.1660G>T	NP_004948.4:p.Ala554Ser
NR_110170.1:n.1708G>T
XM_005251864.2:c.1483+177G>T	XP_005251921.1:n.1483+177G>T
XM_011518437.1:c.1510G>T	XP_011516739.1:p.Ala504Ser
XM_011518438.1:c.1510G>T	XP_011516740.1:p.Ala504Ser
XM_011518439.1:c.817G>T	XP_011516741.1:p.Ala273Ser
XR_242581.2:n.1557G>T
XR_242582.2:n.1380+177G>T
XM_005251864.4:c.1483+177G>T	XP_005251921.1:n.1483+177G>T
XM_011518439.2:c.817G>T	XP_011516741.1:p.Ala273Ser
XM_017014565.2:c.1333+177G>T	XP_016870054.1:n.1333+177G>T
XM_017014566.1:c.817G>T	XP_016870055.1:p.Ala273Ser
XR_242581.4:n.1555G>T
XR_242582.4:n.1378+177G>T
NM_004957.6:c.1660G>T MANE Select	NP_004948.4:p.Ala554Ser