Canonical Allele Identifier: CA1324023477
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326360A= , CM000664.2:g.208326360A= GRCh38
NC_000002.11:g.209191084A= , CM000664.1:g.209191084A= GRCh37
NC_000002.10:g.208899329A= NCBI36
NG_021188.1:g.65094A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3549A= MANE Select ENSP00000264380.4:p.Gln1183=
ENST00000264380.8:c.3549A= ENSP00000264380.4:p.Gln1183=
ENST00000452564.1:c.3381A= ENSP00000405736.1:p.Gln1127=
NM_015040.3:c.3549A= NP_055855.2:p.Gln1183=
XM_011510778.1:c.3585A= XP_011509080.1:p.Gln1195=
XM_011510779.1:c.3585A= XP_011509081.1:p.Gln1195=
XM_011510780.1:c.3582A= XP_011509082.1:p.Gln1194=
XM_011510781.1:c.3567A= XP_011509083.1:p.Gln1189=
XM_011510782.1:c.3585A= XP_011509084.1:p.Gln1195=
XM_011510783.1:c.3417A= XP_011509085.1:p.Gln1139=
XM_011510784.1:c.3414A= XP_011509086.1:p.Gln1138=
XM_011510785.1:c.3399A= XP_011509087.1:p.Gln1133=
XM_011510786.1:c.3294A= XP_011509088.1:p.Gln1098=
XM_011510787.1:c.3291A= XP_011509089.1:p.Gln1097=
XM_011510788.1:c.3258A= XP_011509090.1:p.Gln1086=
XM_011510789.1:c.3108A= XP_011509091.1:p.Gln1036=
XM_011510790.1:c.2592A= XP_011509092.1:p.Gln864=
XM_011510791.1:c.2592A= XP_011509093.1:p.Gln864=
XM_011510792.1:c.3585A= XP_011509094.1:p.Gln1195=
XR_922888.1:n.3722A=
XM_011510778.3:c.3585A= XP_011509080.1:p.Gln1195=
XM_011510779.2:c.3585A= XP_011509081.1:p.Gln1195=
XM_011510780.2:c.3582A= XP_011509082.1:p.Gln1194=
XM_011510781.3:c.3567A= XP_011509083.1:p.Gln1189=
XM_011510782.3:c.3585A= XP_011509084.1:p.Gln1195=
XM_011510783.3:c.3417A= XP_011509085.1:p.Gln1139=
XM_011510784.2:c.3414A= XP_011509086.1:p.Gln1138=
XM_011510785.3:c.3399A= XP_011509087.1:p.Gln1133=
XM_011510786.3:c.3294A= XP_011509088.1:p.Gln1098=
XM_011510789.2:c.3108A= XP_011509091.1:p.Gln1036=
XM_011510792.3:c.3585A= XP_011509094.1:p.Gln1195=
XM_017003568.1:c.3531A= XP_016859057.1:p.Gln1177=
XM_017003569.1:c.3363A= XP_016859058.1:p.Gln1121=
XM_017003570.1:c.3090A= XP_016859059.1:p.Gln1030=
XM_017003571.1:c.2940A= XP_016859060.1:p.Gln980=
XM_017003572.1:c.2592A= XP_016859061.1:p.Gln864=
XM_017003573.1:c.2592A= XP_016859062.1:p.Gln864=
XM_017003574.1:c.2592A= XP_016859063.1:p.Gln864=
NM_015040.4:c.3549A= MANE Select NP_055855.2:p.Gln1183=