Canonical Allele Identifier: CA350115621

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209191009A>T (hg19) ; chr2:g.208326285A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326285A>T , CM000664.2:g.208326285A>T	GRCh38
NC_000002.11:g.209191009A>T , CM000664.1:g.209191009A>T	GRCh37
NC_000002.10:g.208899254A>T	NCBI36
NG_021188.1:g.65019A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3474A>T MANE Select	ENSP00000264380.4:p.Arg1158Ser
ENST00000264380.8:c.3474A>T	ENSP00000264380.4:p.Arg1158Ser
ENST00000452564.1:c.3306A>T	ENSP00000405736.1:p.Arg1102Ser
NM_015040.3:c.3474A>T	NP_055855.2:p.Arg1158Ser
XM_011510778.1:c.3510A>T	XP_011509080.1:p.Arg1170Ser
XM_011510779.1:c.3510A>T	XP_011509081.1:p.Arg1170Ser
XM_011510780.1:c.3507A>T	XP_011509082.1:p.Arg1169Ser
XM_011510781.1:c.3492A>T	XP_011509083.1:p.Arg1164Ser
XM_011510782.1:c.3510A>T	XP_011509084.1:p.Arg1170Ser
XM_011510783.1:c.3342A>T	XP_011509085.1:p.Arg1114Ser
XM_011510784.1:c.3339A>T	XP_011509086.1:p.Arg1113Ser
XM_011510785.1:c.3324A>T	XP_011509087.1:p.Arg1108Ser
XM_011510786.1:c.3219A>T	XP_011509088.1:p.Arg1073Ser
XM_011510787.1:c.3216A>T	XP_011509089.1:p.Arg1072Ser
XM_011510788.1:c.3183A>T	XP_011509090.1:p.Arg1061Ser
XM_011510789.1:c.3033A>T	XP_011509091.1:p.Arg1011Ser
XM_011510790.1:c.2517A>T	XP_011509092.1:p.Arg839Ser
XM_011510791.1:c.2517A>T	XP_011509093.1:p.Arg839Ser
XM_011510792.1:c.3510A>T	XP_011509094.1:p.Arg1170Ser
XR_922888.1:n.3647A>T
XM_011510778.3:c.3510A>T	XP_011509080.1:p.Arg1170Ser
XM_011510779.2:c.3510A>T	XP_011509081.1:p.Arg1170Ser
XM_011510780.2:c.3507A>T	XP_011509082.1:p.Arg1169Ser
XM_011510781.3:c.3492A>T	XP_011509083.1:p.Arg1164Ser
XM_011510782.3:c.3510A>T	XP_011509084.1:p.Arg1170Ser
XM_011510783.3:c.3342A>T	XP_011509085.1:p.Arg1114Ser
XM_011510784.2:c.3339A>T	XP_011509086.1:p.Arg1113Ser
XM_011510785.3:c.3324A>T	XP_011509087.1:p.Arg1108Ser
XM_011510786.3:c.3219A>T	XP_011509088.1:p.Arg1073Ser
XM_011510789.2:c.3033A>T	XP_011509091.1:p.Arg1011Ser
XM_011510792.3:c.3510A>T	XP_011509094.1:p.Arg1170Ser
XM_017003568.1:c.3456A>T	XP_016859057.1:p.Arg1152Ser
XM_017003569.1:c.3288A>T	XP_016859058.1:p.Arg1096Ser
XM_017003570.1:c.3015A>T	XP_016859059.1:p.Arg1005Ser
XM_017003571.1:c.2865A>T	XP_016859060.1:p.Arg955Ser
XM_017003572.1:c.2517A>T	XP_016859061.1:p.Arg839Ser
XM_017003573.1:c.2517A>T	XP_016859062.1:p.Arg839Ser
XM_017003574.1:c.2517A>T	XP_016859063.1:p.Arg839Ser
NM_015040.4:c.3474A>T MANE Select	NP_055855.2:p.Arg1158Ser