Canonical Allele Identifier: CA350115738

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209191062C>A (hg19) ; chr2:g.208326338C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326338C>A , CM000664.2:g.208326338C>A	GRCh38
NC_000002.11:g.209191062C>A , CM000664.1:g.209191062C>A	GRCh37
NC_000002.10:g.208899307C>A	NCBI36
NG_021188.1:g.65072C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3527C>A MANE Select	ENSP00000264380.4:p.Ala1176Glu
ENST00000264380.8:c.3527C>A	ENSP00000264380.4:p.Ala1176Glu
ENST00000452564.1:c.3359C>A	ENSP00000405736.1:p.Ala1120Glu
NM_015040.3:c.3527C>A	NP_055855.2:p.Ala1176Glu
XM_011510778.1:c.3563C>A	XP_011509080.1:p.Ala1188Glu
XM_011510779.1:c.3563C>A	XP_011509081.1:p.Ala1188Glu
XM_011510780.1:c.3560C>A	XP_011509082.1:p.Ala1187Glu
XM_011510781.1:c.3545C>A	XP_011509083.1:p.Ala1182Glu
XM_011510782.1:c.3563C>A	XP_011509084.1:p.Ala1188Glu
XM_011510783.1:c.3395C>A	XP_011509085.1:p.Ala1132Glu
XM_011510784.1:c.3392C>A	XP_011509086.1:p.Ala1131Glu
XM_011510785.1:c.3377C>A	XP_011509087.1:p.Ala1126Glu
XM_011510786.1:c.3272C>A	XP_011509088.1:p.Ala1091Glu
XM_011510787.1:c.3269C>A	XP_011509089.1:p.Ala1090Glu
XM_011510788.1:c.3236C>A	XP_011509090.1:p.Ala1079Glu
XM_011510789.1:c.3086C>A	XP_011509091.1:p.Ala1029Glu
XM_011510790.1:c.2570C>A	XP_011509092.1:p.Ala857Glu
XM_011510791.1:c.2570C>A	XP_011509093.1:p.Ala857Glu
XM_011510792.1:c.3563C>A	XP_011509094.1:p.Ala1188Glu
XR_922888.1:n.3700C>A
XM_011510778.3:c.3563C>A	XP_011509080.1:p.Ala1188Glu
XM_011510779.2:c.3563C>A	XP_011509081.1:p.Ala1188Glu
XM_011510780.2:c.3560C>A	XP_011509082.1:p.Ala1187Glu
XM_011510781.3:c.3545C>A	XP_011509083.1:p.Ala1182Glu
XM_011510782.3:c.3563C>A	XP_011509084.1:p.Ala1188Glu
XM_011510783.3:c.3395C>A	XP_011509085.1:p.Ala1132Glu
XM_011510784.2:c.3392C>A	XP_011509086.1:p.Ala1131Glu
XM_011510785.3:c.3377C>A	XP_011509087.1:p.Ala1126Glu
XM_011510786.3:c.3272C>A	XP_011509088.1:p.Ala1091Glu
XM_011510789.2:c.3086C>A	XP_011509091.1:p.Ala1029Glu
XM_011510792.3:c.3563C>A	XP_011509094.1:p.Ala1188Glu
XM_017003568.1:c.3509C>A	XP_016859057.1:p.Ala1170Glu
XM_017003569.1:c.3341C>A	XP_016859058.1:p.Ala1114Glu
XM_017003570.1:c.3068C>A	XP_016859059.1:p.Ala1023Glu
XM_017003571.1:c.2918C>A	XP_016859060.1:p.Ala973Glu
XM_017003572.1:c.2570C>A	XP_016859061.1:p.Ala857Glu
XM_017003573.1:c.2570C>A	XP_016859062.1:p.Ala857Glu
XM_017003574.1:c.2570C>A	XP_016859063.1:p.Ala857Glu
NM_015040.4:c.3527C>A MANE Select	NP_055855.2:p.Ala1176Glu