Canonical Allele Identifier: CA350115609

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209191004G>T (hg19) ; chr2:g.208326280G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326280G>T , CM000664.2:g.208326280G>T	GRCh38
NC_000002.11:g.209191004G>T , CM000664.1:g.209191004G>T	GRCh37
NC_000002.10:g.208899249G>T	NCBI36
NG_021188.1:g.65014G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3469G>T MANE Select	ENSP00000264380.4:p.Ala1157Ser
ENST00000264380.8:c.3469G>T	ENSP00000264380.4:p.Ala1157Ser
ENST00000452564.1:c.3301G>T	ENSP00000405736.1:p.Ala1101Ser
NM_015040.3:c.3469G>T	NP_055855.2:p.Ala1157Ser
XM_011510778.1:c.3505G>T	XP_011509080.1:p.Ala1169Ser
XM_011510779.1:c.3505G>T	XP_011509081.1:p.Ala1169Ser
XM_011510780.1:c.3502G>T	XP_011509082.1:p.Ala1168Ser
XM_011510781.1:c.3487G>T	XP_011509083.1:p.Ala1163Ser
XM_011510782.1:c.3505G>T	XP_011509084.1:p.Ala1169Ser
XM_011510783.1:c.3337G>T	XP_011509085.1:p.Ala1113Ser
XM_011510784.1:c.3334G>T	XP_011509086.1:p.Ala1112Ser
XM_011510785.1:c.3319G>T	XP_011509087.1:p.Ala1107Ser
XM_011510786.1:c.3214G>T	XP_011509088.1:p.Ala1072Ser
XM_011510787.1:c.3211G>T	XP_011509089.1:p.Ala1071Ser
XM_011510788.1:c.3178G>T	XP_011509090.1:p.Ala1060Ser
XM_011510789.1:c.3028G>T	XP_011509091.1:p.Ala1010Ser
XM_011510790.1:c.2512G>T	XP_011509092.1:p.Ala838Ser
XM_011510791.1:c.2512G>T	XP_011509093.1:p.Ala838Ser
XM_011510792.1:c.3505G>T	XP_011509094.1:p.Ala1169Ser
XR_922888.1:n.3642G>T
XM_011510778.3:c.3505G>T	XP_011509080.1:p.Ala1169Ser
XM_011510779.2:c.3505G>T	XP_011509081.1:p.Ala1169Ser
XM_011510780.2:c.3502G>T	XP_011509082.1:p.Ala1168Ser
XM_011510781.3:c.3487G>T	XP_011509083.1:p.Ala1163Ser
XM_011510782.3:c.3505G>T	XP_011509084.1:p.Ala1169Ser
XM_011510783.3:c.3337G>T	XP_011509085.1:p.Ala1113Ser
XM_011510784.2:c.3334G>T	XP_011509086.1:p.Ala1112Ser
XM_011510785.3:c.3319G>T	XP_011509087.1:p.Ala1107Ser
XM_011510786.3:c.3214G>T	XP_011509088.1:p.Ala1072Ser
XM_011510789.2:c.3028G>T	XP_011509091.1:p.Ala1010Ser
XM_011510792.3:c.3505G>T	XP_011509094.1:p.Ala1169Ser
XM_017003568.1:c.3451G>T	XP_016859057.1:p.Ala1151Ser
XM_017003569.1:c.3283G>T	XP_016859058.1:p.Ala1095Ser
XM_017003570.1:c.3010G>T	XP_016859059.1:p.Ala1004Ser
XM_017003571.1:c.2860G>T	XP_016859060.1:p.Ala954Ser
XM_017003572.1:c.2512G>T	XP_016859061.1:p.Ala838Ser
XM_017003573.1:c.2512G>T	XP_016859062.1:p.Ala838Ser
XM_017003574.1:c.2512G>T	XP_016859063.1:p.Ala838Ser
NM_015040.4:c.3469G>T MANE Select	NP_055855.2:p.Ala1157Ser