Canonical Allele Identifier: CA350115474

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209190942C>T (hg19) ; chr2:g.208326218C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326218C>T , CM000664.2:g.208326218C>T	GRCh38
NC_000002.11:g.209190942C>T , CM000664.1:g.209190942C>T	GRCh37
NC_000002.10:g.208899187C>T	NCBI36
NG_021188.1:g.64952C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3407C>T MANE Select	ENSP00000264380.4:p.Thr1136Ile
ENST00000264380.8:c.3407C>T	ENSP00000264380.4:p.Thr1136Ile
ENST00000452564.1:c.3239C>T	ENSP00000405736.1:p.Thr1080Ile
NM_015040.3:c.3407C>T	NP_055855.2:p.Thr1136Ile
XM_011510778.1:c.3443C>T	XP_011509080.1:p.Thr1148Ile
XM_011510779.1:c.3443C>T	XP_011509081.1:p.Thr1148Ile
XM_011510780.1:c.3440C>T	XP_011509082.1:p.Thr1147Ile
XM_011510781.1:c.3425C>T	XP_011509083.1:p.Thr1142Ile
XM_011510782.1:c.3443C>T	XP_011509084.1:p.Thr1148Ile
XM_011510783.1:c.3275C>T	XP_011509085.1:p.Thr1092Ile
XM_011510784.1:c.3272C>T	XP_011509086.1:p.Thr1091Ile
XM_011510785.1:c.3257C>T	XP_011509087.1:p.Thr1086Ile
XM_011510786.1:c.3152C>T	XP_011509088.1:p.Thr1051Ile
XM_011510787.1:c.3149C>T	XP_011509089.1:p.Thr1050Ile
XM_011510788.1:c.3116C>T	XP_011509090.1:p.Thr1039Ile
XM_011510789.1:c.2966C>T	XP_011509091.1:p.Thr989Ile
XM_011510790.1:c.2450C>T	XP_011509092.1:p.Thr817Ile
XM_011510791.1:c.2450C>T	XP_011509093.1:p.Thr817Ile
XM_011510792.1:c.3443C>T	XP_011509094.1:p.Thr1148Ile
XR_922888.1:n.3580C>T
XM_011510778.3:c.3443C>T	XP_011509080.1:p.Thr1148Ile
XM_011510779.2:c.3443C>T	XP_011509081.1:p.Thr1148Ile
XM_011510780.2:c.3440C>T	XP_011509082.1:p.Thr1147Ile
XM_011510781.3:c.3425C>T	XP_011509083.1:p.Thr1142Ile
XM_011510782.3:c.3443C>T	XP_011509084.1:p.Thr1148Ile
XM_011510783.3:c.3275C>T	XP_011509085.1:p.Thr1092Ile
XM_011510784.2:c.3272C>T	XP_011509086.1:p.Thr1091Ile
XM_011510785.3:c.3257C>T	XP_011509087.1:p.Thr1086Ile
XM_011510786.3:c.3152C>T	XP_011509088.1:p.Thr1051Ile
XM_011510789.2:c.2966C>T	XP_011509091.1:p.Thr989Ile
XM_011510792.3:c.3443C>T	XP_011509094.1:p.Thr1148Ile
XM_017003568.1:c.3389C>T	XP_016859057.1:p.Thr1130Ile
XM_017003569.1:c.3221C>T	XP_016859058.1:p.Thr1074Ile
XM_017003570.1:c.2948C>T	XP_016859059.1:p.Thr983Ile
XM_017003571.1:c.2798C>T	XP_016859060.1:p.Thr933Ile
XM_017003572.1:c.2450C>T	XP_016859061.1:p.Thr817Ile
XM_017003573.1:c.2450C>T	XP_016859062.1:p.Thr817Ile
XM_017003574.1:c.2450C>T	XP_016859063.1:p.Thr817Ile
NM_015040.4:c.3407C>T MANE Select	NP_055855.2:p.Thr1136Ile