Canonical Allele Identifier: CA350115623
Gene: PIKFYVE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326286G>T , CM000664.2:g.208326286G>T GRCh38
NC_000002.11:g.209191010G>T , CM000664.1:g.209191010G>T GRCh37
NC_000002.10:g.208899255G>T NCBI36
NG_021188.1:g.65020G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3475G>T MANE Select ENSP00000264380.4:p.Gly1159Ter
ENST00000264380.8:c.3475G>T ENSP00000264380.4:p.Gly1159Ter
ENST00000452564.1:c.3307G>T ENSP00000405736.1:p.Gly1103Ter
NM_015040.3:c.3475G>T NP_055855.2:p.Gly1159Ter
XM_011510778.1:c.3511G>T XP_011509080.1:p.Gly1171Ter
XM_011510779.1:c.3511G>T XP_011509081.1:p.Gly1171Ter
XM_011510780.1:c.3508G>T XP_011509082.1:p.Gly1170Ter
XM_011510781.1:c.3493G>T XP_011509083.1:p.Gly1165Ter
XM_011510782.1:c.3511G>T XP_011509084.1:p.Gly1171Ter
XM_011510783.1:c.3343G>T XP_011509085.1:p.Gly1115Ter
XM_011510784.1:c.3340G>T XP_011509086.1:p.Gly1114Ter
XM_011510785.1:c.3325G>T XP_011509087.1:p.Gly1109Ter
XM_011510786.1:c.3220G>T XP_011509088.1:p.Gly1074Ter
XM_011510787.1:c.3217G>T XP_011509089.1:p.Gly1073Ter
XM_011510788.1:c.3184G>T XP_011509090.1:p.Gly1062Ter
XM_011510789.1:c.3034G>T XP_011509091.1:p.Gly1012Ter
XM_011510790.1:c.2518G>T XP_011509092.1:p.Gly840Ter
XM_011510791.1:c.2518G>T XP_011509093.1:p.Gly840Ter
XM_011510792.1:c.3511G>T XP_011509094.1:p.Gly1171Ter
XR_922888.1:n.3648G>T
XM_011510778.3:c.3511G>T XP_011509080.1:p.Gly1171Ter
XM_011510779.2:c.3511G>T XP_011509081.1:p.Gly1171Ter
XM_011510780.2:c.3508G>T XP_011509082.1:p.Gly1170Ter
XM_011510781.3:c.3493G>T XP_011509083.1:p.Gly1165Ter
XM_011510782.3:c.3511G>T XP_011509084.1:p.Gly1171Ter
XM_011510783.3:c.3343G>T XP_011509085.1:p.Gly1115Ter
XM_011510784.2:c.3340G>T XP_011509086.1:p.Gly1114Ter
XM_011510785.3:c.3325G>T XP_011509087.1:p.Gly1109Ter
XM_011510786.3:c.3220G>T XP_011509088.1:p.Gly1074Ter
XM_011510789.2:c.3034G>T XP_011509091.1:p.Gly1012Ter
XM_011510792.3:c.3511G>T XP_011509094.1:p.Gly1171Ter
XM_017003568.1:c.3457G>T XP_016859057.1:p.Gly1153Ter
XM_017003569.1:c.3289G>T XP_016859058.1:p.Gly1097Ter
XM_017003570.1:c.3016G>T XP_016859059.1:p.Gly1006Ter
XM_017003571.1:c.2866G>T XP_016859060.1:p.Gly956Ter
XM_017003572.1:c.2518G>T XP_016859061.1:p.Gly840Ter
XM_017003573.1:c.2518G>T XP_016859062.1:p.Gly840Ter
XM_017003574.1:c.2518G>T XP_016859063.1:p.Gly840Ter
NM_015040.4:c.3475G>T MANE Select NP_055855.2:p.Gly1159Ter