Canonical Allele Identifier: CA1324023426
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326240C= , CM000664.2:g.208326240C= GRCh38
NC_000002.11:g.209190964C= , CM000664.1:g.209190964C= GRCh37
NC_000002.10:g.208899209C= NCBI36
NG_021188.1:g.64974C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3429C= MANE Select ENSP00000264380.4:p.Gly1143=
ENST00000264380.8:c.3429C= ENSP00000264380.4:p.Gly1143=
ENST00000452564.1:c.3261C= ENSP00000405736.1:p.Gly1087=
NM_015040.3:c.3429C= NP_055855.2:p.Gly1143=
XM_011510778.1:c.3465C= XP_011509080.1:p.Gly1155=
XM_011510779.1:c.3465C= XP_011509081.1:p.Gly1155=
XM_011510780.1:c.3462C= XP_011509082.1:p.Gly1154=
XM_011510781.1:c.3447C= XP_011509083.1:p.Gly1149=
XM_011510782.1:c.3465C= XP_011509084.1:p.Gly1155=
XM_011510783.1:c.3297C= XP_011509085.1:p.Gly1099=
XM_011510784.1:c.3294C= XP_011509086.1:p.Gly1098=
XM_011510785.1:c.3279C= XP_011509087.1:p.Gly1093=
XM_011510786.1:c.3174C= XP_011509088.1:p.Gly1058=
XM_011510787.1:c.3171C= XP_011509089.1:p.Gly1057=
XM_011510788.1:c.3138C= XP_011509090.1:p.Gly1046=
XM_011510789.1:c.2988C= XP_011509091.1:p.Gly996=
XM_011510790.1:c.2472C= XP_011509092.1:p.Gly824=
XM_011510791.1:c.2472C= XP_011509093.1:p.Gly824=
XM_011510792.1:c.3465C= XP_011509094.1:p.Gly1155=
XR_922888.1:n.3602C=
XM_011510778.3:c.3465C= XP_011509080.1:p.Gly1155=
XM_011510779.2:c.3465C= XP_011509081.1:p.Gly1155=
XM_011510780.2:c.3462C= XP_011509082.1:p.Gly1154=
XM_011510781.3:c.3447C= XP_011509083.1:p.Gly1149=
XM_011510782.3:c.3465C= XP_011509084.1:p.Gly1155=
XM_011510783.3:c.3297C= XP_011509085.1:p.Gly1099=
XM_011510784.2:c.3294C= XP_011509086.1:p.Gly1098=
XM_011510785.3:c.3279C= XP_011509087.1:p.Gly1093=
XM_011510786.3:c.3174C= XP_011509088.1:p.Gly1058=
XM_011510789.2:c.2988C= XP_011509091.1:p.Gly996=
XM_011510792.3:c.3465C= XP_011509094.1:p.Gly1155=
XM_017003568.1:c.3411C= XP_016859057.1:p.Gly1137=
XM_017003569.1:c.3243C= XP_016859058.1:p.Gly1081=
XM_017003570.1:c.2970C= XP_016859059.1:p.Gly990=
XM_017003571.1:c.2820C= XP_016859060.1:p.Gly940=
XM_017003572.1:c.2472C= XP_016859061.1:p.Gly824=
XM_017003573.1:c.2472C= XP_016859062.1:p.Gly824=
XM_017003574.1:c.2472C= XP_016859063.1:p.Gly824=
NM_015040.4:c.3429C= MANE Select NP_055855.2:p.Gly1143=