Canonical Allele Identifier: CA350115481

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209190946A>T (hg19) ; chr2:g.208326222A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326222A>T , CM000664.2:g.208326222A>T	GRCh38
NC_000002.11:g.209190946A>T , CM000664.1:g.209190946A>T	GRCh37
NC_000002.10:g.208899191A>T	NCBI36
NG_021188.1:g.64956A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3411A>T MANE Select	ENSP00000264380.4:p.Arg1137Ser
ENST00000264380.8:c.3411A>T	ENSP00000264380.4:p.Arg1137Ser
ENST00000452564.1:c.3243A>T	ENSP00000405736.1:p.Arg1081Ser
NM_015040.3:c.3411A>T	NP_055855.2:p.Arg1137Ser
XM_011510778.1:c.3447A>T	XP_011509080.1:p.Arg1149Ser
XM_011510779.1:c.3447A>T	XP_011509081.1:p.Arg1149Ser
XM_011510780.1:c.3444A>T	XP_011509082.1:p.Arg1148Ser
XM_011510781.1:c.3429A>T	XP_011509083.1:p.Arg1143Ser
XM_011510782.1:c.3447A>T	XP_011509084.1:p.Arg1149Ser
XM_011510783.1:c.3279A>T	XP_011509085.1:p.Arg1093Ser
XM_011510784.1:c.3276A>T	XP_011509086.1:p.Arg1092Ser
XM_011510785.1:c.3261A>T	XP_011509087.1:p.Arg1087Ser
XM_011510786.1:c.3156A>T	XP_011509088.1:p.Arg1052Ser
XM_011510787.1:c.3153A>T	XP_011509089.1:p.Arg1051Ser
XM_011510788.1:c.3120A>T	XP_011509090.1:p.Arg1040Ser
XM_011510789.1:c.2970A>T	XP_011509091.1:p.Arg990Ser
XM_011510790.1:c.2454A>T	XP_011509092.1:p.Arg818Ser
XM_011510791.1:c.2454A>T	XP_011509093.1:p.Arg818Ser
XM_011510792.1:c.3447A>T	XP_011509094.1:p.Arg1149Ser
XR_922888.1:n.3584A>T
XM_011510778.3:c.3447A>T	XP_011509080.1:p.Arg1149Ser
XM_011510779.2:c.3447A>T	XP_011509081.1:p.Arg1149Ser
XM_011510780.2:c.3444A>T	XP_011509082.1:p.Arg1148Ser
XM_011510781.3:c.3429A>T	XP_011509083.1:p.Arg1143Ser
XM_011510782.3:c.3447A>T	XP_011509084.1:p.Arg1149Ser
XM_011510783.3:c.3279A>T	XP_011509085.1:p.Arg1093Ser
XM_011510784.2:c.3276A>T	XP_011509086.1:p.Arg1092Ser
XM_011510785.3:c.3261A>T	XP_011509087.1:p.Arg1087Ser
XM_011510786.3:c.3156A>T	XP_011509088.1:p.Arg1052Ser
XM_011510789.2:c.2970A>T	XP_011509091.1:p.Arg990Ser
XM_011510792.3:c.3447A>T	XP_011509094.1:p.Arg1149Ser
XM_017003568.1:c.3393A>T	XP_016859057.1:p.Arg1131Ser
XM_017003569.1:c.3225A>T	XP_016859058.1:p.Arg1075Ser
XM_017003570.1:c.2952A>T	XP_016859059.1:p.Arg984Ser
XM_017003571.1:c.2802A>T	XP_016859060.1:p.Arg934Ser
XM_017003572.1:c.2454A>T	XP_016859061.1:p.Arg818Ser
XM_017003573.1:c.2454A>T	XP_016859062.1:p.Arg818Ser
XM_017003574.1:c.2454A>T	XP_016859063.1:p.Arg818Ser
NM_015040.4:c.3411A>T MANE Select	NP_055855.2:p.Arg1137Ser