Canonical Allele Identifier: CA1324023437
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326253T= , CM000664.2:g.208326253T= GRCh38
NC_000002.11:g.209190977T= , CM000664.1:g.209190977T= GRCh37
NC_000002.10:g.208899222T= NCBI36
NG_021188.1:g.64987T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3442T= MANE Select ENSP00000264380.4:p.Leu1148=
ENST00000264380.8:c.3442T= ENSP00000264380.4:p.Leu1148=
ENST00000452564.1:c.3274T= ENSP00000405736.1:p.Leu1092=
NM_015040.3:c.3442T= NP_055855.2:p.Leu1148=
XM_011510778.1:c.3478T= XP_011509080.1:p.Leu1160=
XM_011510779.1:c.3478T= XP_011509081.1:p.Leu1160=
XM_011510780.1:c.3475T= XP_011509082.1:p.Leu1159=
XM_011510781.1:c.3460T= XP_011509083.1:p.Leu1154=
XM_011510782.1:c.3478T= XP_011509084.1:p.Leu1160=
XM_011510783.1:c.3310T= XP_011509085.1:p.Leu1104=
XM_011510784.1:c.3307T= XP_011509086.1:p.Leu1103=
XM_011510785.1:c.3292T= XP_011509087.1:p.Leu1098=
XM_011510786.1:c.3187T= XP_011509088.1:p.Leu1063=
XM_011510787.1:c.3184T= XP_011509089.1:p.Leu1062=
XM_011510788.1:c.3151T= XP_011509090.1:p.Leu1051=
XM_011510789.1:c.3001T= XP_011509091.1:p.Leu1001=
XM_011510790.1:c.2485T= XP_011509092.1:p.Leu829=
XM_011510791.1:c.2485T= XP_011509093.1:p.Leu829=
XM_011510792.1:c.3478T= XP_011509094.1:p.Leu1160=
XR_922888.1:n.3615T=
XM_011510778.3:c.3478T= XP_011509080.1:p.Leu1160=
XM_011510779.2:c.3478T= XP_011509081.1:p.Leu1160=
XM_011510780.2:c.3475T= XP_011509082.1:p.Leu1159=
XM_011510781.3:c.3460T= XP_011509083.1:p.Leu1154=
XM_011510782.3:c.3478T= XP_011509084.1:p.Leu1160=
XM_011510783.3:c.3310T= XP_011509085.1:p.Leu1104=
XM_011510784.2:c.3307T= XP_011509086.1:p.Leu1103=
XM_011510785.3:c.3292T= XP_011509087.1:p.Leu1098=
XM_011510786.3:c.3187T= XP_011509088.1:p.Leu1063=
XM_011510789.2:c.3001T= XP_011509091.1:p.Leu1001=
XM_011510792.3:c.3478T= XP_011509094.1:p.Leu1160=
XM_017003568.1:c.3424T= XP_016859057.1:p.Leu1142=
XM_017003569.1:c.3256T= XP_016859058.1:p.Leu1086=
XM_017003570.1:c.2983T= XP_016859059.1:p.Leu995=
XM_017003571.1:c.2833T= XP_016859060.1:p.Leu945=
XM_017003572.1:c.2485T= XP_016859061.1:p.Leu829=
XM_017003573.1:c.2485T= XP_016859062.1:p.Leu829=
XM_017003574.1:c.2485T= XP_016859063.1:p.Leu829=
NM_015040.4:c.3442T= MANE Select NP_055855.2:p.Leu1148=