Canonical Allele Identifier: CA1324023432
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326249G= , CM000664.2:g.208326249G= GRCh38
NC_000002.11:g.209190973G= , CM000664.1:g.209190973G= GRCh37
NC_000002.10:g.208899218G= NCBI36
NG_021188.1:g.64983G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3438G= MANE Select ENSP00000264380.4:p.Gln1146=
ENST00000264380.8:c.3438G= ENSP00000264380.4:p.Gln1146=
ENST00000452564.1:c.3270G= ENSP00000405736.1:p.Gln1090=
NM_015040.3:c.3438G= NP_055855.2:p.Gln1146=
XM_011510778.1:c.3474G= XP_011509080.1:p.Gln1158=
XM_011510779.1:c.3474G= XP_011509081.1:p.Gln1158=
XM_011510780.1:c.3471G= XP_011509082.1:p.Gln1157=
XM_011510781.1:c.3456G= XP_011509083.1:p.Gln1152=
XM_011510782.1:c.3474G= XP_011509084.1:p.Gln1158=
XM_011510783.1:c.3306G= XP_011509085.1:p.Gln1102=
XM_011510784.1:c.3303G= XP_011509086.1:p.Gln1101=
XM_011510785.1:c.3288G= XP_011509087.1:p.Gln1096=
XM_011510786.1:c.3183G= XP_011509088.1:p.Gln1061=
XM_011510787.1:c.3180G= XP_011509089.1:p.Gln1060=
XM_011510788.1:c.3147G= XP_011509090.1:p.Gln1049=
XM_011510789.1:c.2997G= XP_011509091.1:p.Gln999=
XM_011510790.1:c.2481G= XP_011509092.1:p.Gln827=
XM_011510791.1:c.2481G= XP_011509093.1:p.Gln827=
XM_011510792.1:c.3474G= XP_011509094.1:p.Gln1158=
XR_922888.1:n.3611G=
XM_011510778.3:c.3474G= XP_011509080.1:p.Gln1158=
XM_011510779.2:c.3474G= XP_011509081.1:p.Gln1158=
XM_011510780.2:c.3471G= XP_011509082.1:p.Gln1157=
XM_011510781.3:c.3456G= XP_011509083.1:p.Gln1152=
XM_011510782.3:c.3474G= XP_011509084.1:p.Gln1158=
XM_011510783.3:c.3306G= XP_011509085.1:p.Gln1102=
XM_011510784.2:c.3303G= XP_011509086.1:p.Gln1101=
XM_011510785.3:c.3288G= XP_011509087.1:p.Gln1096=
XM_011510786.3:c.3183G= XP_011509088.1:p.Gln1061=
XM_011510789.2:c.2997G= XP_011509091.1:p.Gln999=
XM_011510792.3:c.3474G= XP_011509094.1:p.Gln1158=
XM_017003568.1:c.3420G= XP_016859057.1:p.Gln1140=
XM_017003569.1:c.3252G= XP_016859058.1:p.Gln1084=
XM_017003570.1:c.2979G= XP_016859059.1:p.Gln993=
XM_017003571.1:c.2829G= XP_016859060.1:p.Gln943=
XM_017003572.1:c.2481G= XP_016859061.1:p.Gln827=
XM_017003573.1:c.2481G= XP_016859062.1:p.Gln827=
XM_017003574.1:c.2481G= XP_016859063.1:p.Gln827=
NM_015040.4:c.3438G= MANE Select NP_055855.2:p.Gln1146=