Canonical Allele Identifier: CA350115502

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209190955G>T (hg19) ; chr2:g.208326231G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326231G>T , CM000664.2:g.208326231G>T	GRCh38
NC_000002.11:g.209190955G>T , CM000664.1:g.209190955G>T	GRCh37
NC_000002.10:g.208899200G>T	NCBI36
NG_021188.1:g.64965G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3420G>T MANE Select	ENSP00000264380.4:p.Glu1140Asp
ENST00000264380.8:c.3420G>T	ENSP00000264380.4:p.Glu1140Asp
ENST00000452564.1:c.3252G>T	ENSP00000405736.1:p.Glu1084Asp
NM_015040.3:c.3420G>T	NP_055855.2:p.Glu1140Asp
XM_011510778.1:c.3456G>T	XP_011509080.1:p.Glu1152Asp
XM_011510779.1:c.3456G>T	XP_011509081.1:p.Glu1152Asp
XM_011510780.1:c.3453G>T	XP_011509082.1:p.Glu1151Asp
XM_011510781.1:c.3438G>T	XP_011509083.1:p.Glu1146Asp
XM_011510782.1:c.3456G>T	XP_011509084.1:p.Glu1152Asp
XM_011510783.1:c.3288G>T	XP_011509085.1:p.Glu1096Asp
XM_011510784.1:c.3285G>T	XP_011509086.1:p.Glu1095Asp
XM_011510785.1:c.3270G>T	XP_011509087.1:p.Glu1090Asp
XM_011510786.1:c.3165G>T	XP_011509088.1:p.Glu1055Asp
XM_011510787.1:c.3162G>T	XP_011509089.1:p.Glu1054Asp
XM_011510788.1:c.3129G>T	XP_011509090.1:p.Glu1043Asp
XM_011510789.1:c.2979G>T	XP_011509091.1:p.Glu993Asp
XM_011510790.1:c.2463G>T	XP_011509092.1:p.Glu821Asp
XM_011510791.1:c.2463G>T	XP_011509093.1:p.Glu821Asp
XM_011510792.1:c.3456G>T	XP_011509094.1:p.Glu1152Asp
XR_922888.1:n.3593G>T
XM_011510778.3:c.3456G>T	XP_011509080.1:p.Glu1152Asp
XM_011510779.2:c.3456G>T	XP_011509081.1:p.Glu1152Asp
XM_011510780.2:c.3453G>T	XP_011509082.1:p.Glu1151Asp
XM_011510781.3:c.3438G>T	XP_011509083.1:p.Glu1146Asp
XM_011510782.3:c.3456G>T	XP_011509084.1:p.Glu1152Asp
XM_011510783.3:c.3288G>T	XP_011509085.1:p.Glu1096Asp
XM_011510784.2:c.3285G>T	XP_011509086.1:p.Glu1095Asp
XM_011510785.3:c.3270G>T	XP_011509087.1:p.Glu1090Asp
XM_011510786.3:c.3165G>T	XP_011509088.1:p.Glu1055Asp
XM_011510789.2:c.2979G>T	XP_011509091.1:p.Glu993Asp
XM_011510792.3:c.3456G>T	XP_011509094.1:p.Glu1152Asp
XM_017003568.1:c.3402G>T	XP_016859057.1:p.Glu1134Asp
XM_017003569.1:c.3234G>T	XP_016859058.1:p.Glu1078Asp
XM_017003570.1:c.2961G>T	XP_016859059.1:p.Glu987Asp
XM_017003571.1:c.2811G>T	XP_016859060.1:p.Glu937Asp
XM_017003572.1:c.2463G>T	XP_016859061.1:p.Glu821Asp
XM_017003573.1:c.2463G>T	XP_016859062.1:p.Glu821Asp
XM_017003574.1:c.2463G>T	XP_016859063.1:p.Glu821Asp
NM_015040.4:c.3420G>T MANE Select	NP_055855.2:p.Glu1140Asp