Canonical Allele Identifier: CA1324023442
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326271G= , CM000664.2:g.208326271G= GRCh38
NC_000002.11:g.209190995G= , CM000664.1:g.209190995G= GRCh37
NC_000002.10:g.208899240G= NCBI36
NG_021188.1:g.65005G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3460G= MANE Select ENSP00000264380.4:p.Asp1154=
ENST00000264380.8:c.3460G= ENSP00000264380.4:p.Asp1154=
ENST00000452564.1:c.3292G= ENSP00000405736.1:p.Asp1098=
NM_015040.3:c.3460G= NP_055855.2:p.Asp1154=
XM_011510778.1:c.3496G= XP_011509080.1:p.Asp1166=
XM_011510779.1:c.3496G= XP_011509081.1:p.Asp1166=
XM_011510780.1:c.3493G= XP_011509082.1:p.Asp1165=
XM_011510781.1:c.3478G= XP_011509083.1:p.Asp1160=
XM_011510782.1:c.3496G= XP_011509084.1:p.Asp1166=
XM_011510783.1:c.3328G= XP_011509085.1:p.Asp1110=
XM_011510784.1:c.3325G= XP_011509086.1:p.Asp1109=
XM_011510785.1:c.3310G= XP_011509087.1:p.Asp1104=
XM_011510786.1:c.3205G= XP_011509088.1:p.Asp1069=
XM_011510787.1:c.3202G= XP_011509089.1:p.Asp1068=
XM_011510788.1:c.3169G= XP_011509090.1:p.Asp1057=
XM_011510789.1:c.3019G= XP_011509091.1:p.Asp1007=
XM_011510790.1:c.2503G= XP_011509092.1:p.Asp835=
XM_011510791.1:c.2503G= XP_011509093.1:p.Asp835=
XM_011510792.1:c.3496G= XP_011509094.1:p.Asp1166=
XR_922888.1:n.3633G=
XM_011510778.3:c.3496G= XP_011509080.1:p.Asp1166=
XM_011510779.2:c.3496G= XP_011509081.1:p.Asp1166=
XM_011510780.2:c.3493G= XP_011509082.1:p.Asp1165=
XM_011510781.3:c.3478G= XP_011509083.1:p.Asp1160=
XM_011510782.3:c.3496G= XP_011509084.1:p.Asp1166=
XM_011510783.3:c.3328G= XP_011509085.1:p.Asp1110=
XM_011510784.2:c.3325G= XP_011509086.1:p.Asp1109=
XM_011510785.3:c.3310G= XP_011509087.1:p.Asp1104=
XM_011510786.3:c.3205G= XP_011509088.1:p.Asp1069=
XM_011510789.2:c.3019G= XP_011509091.1:p.Asp1007=
XM_011510792.3:c.3496G= XP_011509094.1:p.Asp1166=
XM_017003568.1:c.3442G= XP_016859057.1:p.Asp1148=
XM_017003569.1:c.3274G= XP_016859058.1:p.Asp1092=
XM_017003570.1:c.3001G= XP_016859059.1:p.Asp1001=
XM_017003571.1:c.2851G= XP_016859060.1:p.Asp951=
XM_017003572.1:c.2503G= XP_016859061.1:p.Asp835=
XM_017003573.1:c.2503G= XP_016859062.1:p.Asp835=
XM_017003574.1:c.2503G= XP_016859063.1:p.Asp835=
NM_015040.4:c.3460G= MANE Select NP_055855.2:p.Asp1154=