Canonical Allele Identifier: CA350115826

Gene: PIKFYVE

Linked Data

• gnomAD v4: 2-208326379-G-A
• MyVariant Identifiers: chr2:g.209191103G>A (hg19) ; chr2:g.208326379G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326379G>A , CM000664.2:g.208326379G>A	GRCh38
NC_000002.11:g.209191103G>A , CM000664.1:g.209191103G>A	GRCh37
NC_000002.10:g.208899348G>A	NCBI36
NG_021188.1:g.65113G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3568G>A MANE Select	ENSP00000264380.4:p.Gly1190Ser
ENST00000264380.8:c.3568G>A	ENSP00000264380.4:p.Gly1190Ser
ENST00000452564.1:c.3400G>A	ENSP00000405736.1:p.Gly1134Ser
NM_015040.3:c.3568G>A	NP_055855.2:p.Gly1190Ser
XM_011510778.1:c.3604G>A	XP_011509080.1:p.Gly1202Ser
XM_011510779.1:c.3604G>A	XP_011509081.1:p.Gly1202Ser
XM_011510780.1:c.3601G>A	XP_011509082.1:p.Gly1201Ser
XM_011510781.1:c.3586G>A	XP_011509083.1:p.Gly1196Ser
XM_011510782.1:c.3604G>A	XP_011509084.1:p.Gly1202Ser
XM_011510783.1:c.3436G>A	XP_011509085.1:p.Gly1146Ser
XM_011510784.1:c.3433G>A	XP_011509086.1:p.Gly1145Ser
XM_011510785.1:c.3418G>A	XP_011509087.1:p.Gly1140Ser
XM_011510786.1:c.3313G>A	XP_011509088.1:p.Gly1105Ser
XM_011510787.1:c.3310G>A	XP_011509089.1:p.Gly1104Ser
XM_011510788.1:c.3277G>A	XP_011509090.1:p.Gly1093Ser
XM_011510789.1:c.3127G>A	XP_011509091.1:p.Gly1043Ser
XM_011510790.1:c.2611G>A	XP_011509092.1:p.Gly871Ser
XM_011510791.1:c.2611G>A	XP_011509093.1:p.Gly871Ser
XM_011510792.1:c.3604G>A	XP_011509094.1:p.Gly1202Ser
XR_922888.1:n.3741G>A
XM_011510778.3:c.3604G>A	XP_011509080.1:p.Gly1202Ser
XM_011510779.2:c.3604G>A	XP_011509081.1:p.Gly1202Ser
XM_011510780.2:c.3601G>A	XP_011509082.1:p.Gly1201Ser
XM_011510781.3:c.3586G>A	XP_011509083.1:p.Gly1196Ser
XM_011510782.3:c.3604G>A	XP_011509084.1:p.Gly1202Ser
XM_011510783.3:c.3436G>A	XP_011509085.1:p.Gly1146Ser
XM_011510784.2:c.3433G>A	XP_011509086.1:p.Gly1145Ser
XM_011510785.3:c.3418G>A	XP_011509087.1:p.Gly1140Ser
XM_011510786.3:c.3313G>A	XP_011509088.1:p.Gly1105Ser
XM_011510789.2:c.3127G>A	XP_011509091.1:p.Gly1043Ser
XM_011510792.3:c.3604G>A	XP_011509094.1:p.Gly1202Ser
XM_017003568.1:c.3550G>A	XP_016859057.1:p.Gly1184Ser
XM_017003569.1:c.3382G>A	XP_016859058.1:p.Gly1128Ser
XM_017003570.1:c.3109G>A	XP_016859059.1:p.Gly1037Ser
XM_017003571.1:c.2959G>A	XP_016859060.1:p.Gly987Ser
XM_017003572.1:c.2611G>A	XP_016859061.1:p.Gly871Ser
XM_017003573.1:c.2611G>A	XP_016859062.1:p.Gly871Ser
XM_017003574.1:c.2611G>A	XP_016859063.1:p.Gly871Ser
NM_015040.4:c.3568G>A MANE Select	NP_055855.2:p.Gly1190Ser