Canonical Allele Identifier: CA374964958

Gene: FPGS

Linked Data

• MyVariant Identifiers: chr9:g.130575623C>A (hg19) ; chr9:g.127813344C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813344C>A , CM000671.2:g.127813344C>A	GRCh38
NC_000009.11:g.130575623C>A , CM000671.1:g.130575623C>A	GRCh37
NC_000009.10:g.129615444C>A	NCBI36
NG_009551.1:g.46425G>T , LRG_589:g.46425G>T
NG_023245.1:g.15470C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1504C>A MANE Select	ENSP00000362344.2:p.Leu502Met
ENST00000373225.7:c.1354C>A	ENSP00000362322.3:p.Leu452Met
ENST00000373228.5:c.*161C>A	ENSP00000362325.1:n.*161C>A
ENST00000373247.6:c.1504C>A	ENSP00000362344.2:p.Leu502Met
ENST00000393706.6:c.1426C>A	ENSP00000377309.2:p.Leu476Met
ENST00000460181.5:n.1492C>A
ENST00000467826.5:n.709+21C>A
ENST00000475270.1:n.330C>A
ENST00000630236.2:c.*228C>A	ENSP00000486766.1:n.*228C>A
NM_001018078.2:c.1354C>A	NP_001018088.1:p.Leu452Met
NM_001288803.1:c.1426C>A	NP_001275732.1:p.Leu476Met
NM_004957.5:c.1504C>A	NP_004948.4:p.Leu502Met
NR_110170.1:n.1552C>A
XM_005251864.2:c.1483+21C>A	XP_005251921.1:n.1483+21C>A
XM_011518437.1:c.1354C>A	XP_011516739.1:p.Leu452Met
XM_011518438.1:c.1354C>A	XP_011516740.1:p.Leu452Met
XM_011518439.1:c.661C>A	XP_011516741.1:p.Leu221Met
XR_242581.2:n.1401C>A
XR_242582.2:n.1380+21C>A
XM_005251864.4:c.1483+21C>A	XP_005251921.1:n.1483+21C>A
XM_011518439.2:c.661C>A	XP_011516741.1:p.Leu221Met
XM_017014565.2:c.1333+21C>A	XP_016870054.1:n.1333+21C>A
XM_017014566.1:c.661C>A	XP_016870055.1:p.Leu221Met
XR_242581.4:n.1399C>A
XR_242582.4:n.1378+21C>A
NM_004957.6:c.1504C>A MANE Select	NP_004948.4:p.Leu502Met