Canonical Allele Identifier: CA1324023416
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326216C= , CM000664.2:g.208326216C= GRCh38
NC_000002.11:g.209190940C= , CM000664.1:g.209190940C= GRCh37
NC_000002.10:g.208899185C= NCBI36
NG_021188.1:g.64950C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3405C= MANE Select ENSP00000264380.4:p.Ser1135=
ENST00000264380.8:c.3405C= ENSP00000264380.4:p.Ser1135=
ENST00000452564.1:c.3237C= ENSP00000405736.1:p.Ser1079=
NM_015040.3:c.3405C= NP_055855.2:p.Ser1135=
XM_011510778.1:c.3441C= XP_011509080.1:p.Ser1147=
XM_011510779.1:c.3441C= XP_011509081.1:p.Ser1147=
XM_011510780.1:c.3438C= XP_011509082.1:p.Ser1146=
XM_011510781.1:c.3423C= XP_011509083.1:p.Ser1141=
XM_011510782.1:c.3441C= XP_011509084.1:p.Ser1147=
XM_011510783.1:c.3273C= XP_011509085.1:p.Ser1091=
XM_011510784.1:c.3270C= XP_011509086.1:p.Ser1090=
XM_011510785.1:c.3255C= XP_011509087.1:p.Ser1085=
XM_011510786.1:c.3150C= XP_011509088.1:p.Ser1050=
XM_011510787.1:c.3147C= XP_011509089.1:p.Ser1049=
XM_011510788.1:c.3114C= XP_011509090.1:p.Ser1038=
XM_011510789.1:c.2964C= XP_011509091.1:p.Ser988=
XM_011510790.1:c.2448C= XP_011509092.1:p.Ser816=
XM_011510791.1:c.2448C= XP_011509093.1:p.Ser816=
XM_011510792.1:c.3441C= XP_011509094.1:p.Ser1147=
XR_922888.1:n.3578C=
XM_011510778.3:c.3441C= XP_011509080.1:p.Ser1147=
XM_011510779.2:c.3441C= XP_011509081.1:p.Ser1147=
XM_011510780.2:c.3438C= XP_011509082.1:p.Ser1146=
XM_011510781.3:c.3423C= XP_011509083.1:p.Ser1141=
XM_011510782.3:c.3441C= XP_011509084.1:p.Ser1147=
XM_011510783.3:c.3273C= XP_011509085.1:p.Ser1091=
XM_011510784.2:c.3270C= XP_011509086.1:p.Ser1090=
XM_011510785.3:c.3255C= XP_011509087.1:p.Ser1085=
XM_011510786.3:c.3150C= XP_011509088.1:p.Ser1050=
XM_011510789.2:c.2964C= XP_011509091.1:p.Ser988=
XM_011510792.3:c.3441C= XP_011509094.1:p.Ser1147=
XM_017003568.1:c.3387C= XP_016859057.1:p.Ser1129=
XM_017003569.1:c.3219C= XP_016859058.1:p.Ser1073=
XM_017003570.1:c.2946C= XP_016859059.1:p.Ser982=
XM_017003571.1:c.2796C= XP_016859060.1:p.Ser932=
XM_017003572.1:c.2448C= XP_016859061.1:p.Ser816=
XM_017003573.1:c.2448C= XP_016859062.1:p.Ser816=
XM_017003574.1:c.2448C= XP_016859063.1:p.Ser816=
NM_015040.4:c.3405C= MANE Select NP_055855.2:p.Ser1135=