Canonical Allele Identifier: CA374966743

Gene: FPGS

Linked Data

• MyVariant Identifiers: chr9:g.130575800G>C (hg19) ; chr9:g.127813521G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813521G>C , CM000671.2:g.127813521G>C	GRCh38
NC_000009.11:g.130575800G>C , CM000671.1:g.130575800G>C	GRCh37
NC_000009.10:g.129615621G>C	NCBI36
NG_009551.1:g.46248C>G , LRG_589:g.46248C>G
NG_023245.1:g.15647G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1681G>C MANE Select	ENSP00000362344.2:p.Ala561Pro
ENST00000373225.7:c.1531G>C	ENSP00000362322.3:p.Ala511Pro
ENST00000373247.6:c.1681G>C	ENSP00000362344.2:p.Ala561Pro
ENST00000393706.6:c.1603G>C	ENSP00000377309.2:p.Ala535Pro
ENST00000460181.5:n.1669G>C
ENST00000467826.5:n.709+198G>C
ENST00000475270.1:n.507G>C
ENST00000630236.2:c.*405G>C	ENSP00000486766.1:n.*405G>C
NM_001018078.2:c.1531G>C	NP_001018088.1:p.Ala511Pro
NM_001288803.1:c.1603G>C	NP_001275732.1:p.Ala535Pro
NM_004957.5:c.1681G>C	NP_004948.4:p.Ala561Pro
NR_110170.1:n.1729G>C
XM_005251864.2:c.1483+198G>C	XP_005251921.1:n.1483+198G>C
XM_011518437.1:c.1531G>C	XP_011516739.1:p.Ala511Pro
XM_011518438.1:c.1531G>C	XP_011516740.1:p.Ala511Pro
XM_011518439.1:c.838G>C	XP_011516741.1:p.Ala280Pro
XR_242581.2:n.1578G>C
XR_242582.2:n.1380+198G>C
XM_005251864.4:c.1483+198G>C	XP_005251921.1:n.1483+198G>C
XM_011518439.2:c.838G>C	XP_011516741.1:p.Ala280Pro
XM_017014565.2:c.1333+198G>C	XP_016870054.1:n.1333+198G>C
XM_017014566.1:c.838G>C	XP_016870055.1:p.Ala280Pro
XR_242581.4:n.1576G>C
XR_242582.4:n.1378+198G>C
NM_004957.6:c.1681G>C MANE Select	NP_004948.4:p.Ala561Pro