Canonical Allele Identifier: CA350115610
Gene: PIKFYVE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326280G>C , CM000664.2:g.208326280G>C GRCh38
NC_000002.11:g.209191004G>C , CM000664.1:g.209191004G>C GRCh37
NC_000002.10:g.208899249G>C NCBI36
NG_021188.1:g.65014G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3469G>C MANE Select ENSP00000264380.4:p.Ala1157Pro
ENST00000264380.8:c.3469G>C ENSP00000264380.4:p.Ala1157Pro
ENST00000452564.1:c.3301G>C ENSP00000405736.1:p.Ala1101Pro
NM_015040.3:c.3469G>C NP_055855.2:p.Ala1157Pro
XM_011510778.1:c.3505G>C XP_011509080.1:p.Ala1169Pro
XM_011510779.1:c.3505G>C XP_011509081.1:p.Ala1169Pro
XM_011510780.1:c.3502G>C XP_011509082.1:p.Ala1168Pro
XM_011510781.1:c.3487G>C XP_011509083.1:p.Ala1163Pro
XM_011510782.1:c.3505G>C XP_011509084.1:p.Ala1169Pro
XM_011510783.1:c.3337G>C XP_011509085.1:p.Ala1113Pro
XM_011510784.1:c.3334G>C XP_011509086.1:p.Ala1112Pro
XM_011510785.1:c.3319G>C XP_011509087.1:p.Ala1107Pro
XM_011510786.1:c.3214G>C XP_011509088.1:p.Ala1072Pro
XM_011510787.1:c.3211G>C XP_011509089.1:p.Ala1071Pro
XM_011510788.1:c.3178G>C XP_011509090.1:p.Ala1060Pro
XM_011510789.1:c.3028G>C XP_011509091.1:p.Ala1010Pro
XM_011510790.1:c.2512G>C XP_011509092.1:p.Ala838Pro
XM_011510791.1:c.2512G>C XP_011509093.1:p.Ala838Pro
XM_011510792.1:c.3505G>C XP_011509094.1:p.Ala1169Pro
XR_922888.1:n.3642G>C
XM_011510778.3:c.3505G>C XP_011509080.1:p.Ala1169Pro
XM_011510779.2:c.3505G>C XP_011509081.1:p.Ala1169Pro
XM_011510780.2:c.3502G>C XP_011509082.1:p.Ala1168Pro
XM_011510781.3:c.3487G>C XP_011509083.1:p.Ala1163Pro
XM_011510782.3:c.3505G>C XP_011509084.1:p.Ala1169Pro
XM_011510783.3:c.3337G>C XP_011509085.1:p.Ala1113Pro
XM_011510784.2:c.3334G>C XP_011509086.1:p.Ala1112Pro
XM_011510785.3:c.3319G>C XP_011509087.1:p.Ala1107Pro
XM_011510786.3:c.3214G>C XP_011509088.1:p.Ala1072Pro
XM_011510789.2:c.3028G>C XP_011509091.1:p.Ala1010Pro
XM_011510792.3:c.3505G>C XP_011509094.1:p.Ala1169Pro
XM_017003568.1:c.3451G>C XP_016859057.1:p.Ala1151Pro
XM_017003569.1:c.3283G>C XP_016859058.1:p.Ala1095Pro
XM_017003570.1:c.3010G>C XP_016859059.1:p.Ala1004Pro
XM_017003571.1:c.2860G>C XP_016859060.1:p.Ala954Pro
XM_017003572.1:c.2512G>C XP_016859061.1:p.Ala838Pro
XM_017003573.1:c.2512G>C XP_016859062.1:p.Ala838Pro
XM_017003574.1:c.2512G>C XP_016859063.1:p.Ala838Pro
NM_015040.4:c.3469G>C MANE Select NP_055855.2:p.Ala1157Pro