Canonical Allele Identifier: CA1324023448
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326293G= , CM000664.2:g.208326293G= GRCh38
NC_000002.11:g.209191017G= , CM000664.1:g.209191017G= GRCh37
NC_000002.10:g.208899262G= NCBI36
NG_021188.1:g.65027G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3482G= MANE Select ENSP00000264380.4:p.Arg1161=
ENST00000264380.8:c.3482G= ENSP00000264380.4:p.Arg1161=
ENST00000452564.1:c.3314G= ENSP00000405736.1:p.Arg1105=
NM_015040.3:c.3482G= NP_055855.2:p.Arg1161=
XM_011510778.1:c.3518G= XP_011509080.1:p.Arg1173=
XM_011510779.1:c.3518G= XP_011509081.1:p.Arg1173=
XM_011510780.1:c.3515G= XP_011509082.1:p.Arg1172=
XM_011510781.1:c.3500G= XP_011509083.1:p.Arg1167=
XM_011510782.1:c.3518G= XP_011509084.1:p.Arg1173=
XM_011510783.1:c.3350G= XP_011509085.1:p.Arg1117=
XM_011510784.1:c.3347G= XP_011509086.1:p.Arg1116=
XM_011510785.1:c.3332G= XP_011509087.1:p.Arg1111=
XM_011510786.1:c.3227G= XP_011509088.1:p.Arg1076=
XM_011510787.1:c.3224G= XP_011509089.1:p.Arg1075=
XM_011510788.1:c.3191G= XP_011509090.1:p.Arg1064=
XM_011510789.1:c.3041G= XP_011509091.1:p.Arg1014=
XM_011510790.1:c.2525G= XP_011509092.1:p.Arg842=
XM_011510791.1:c.2525G= XP_011509093.1:p.Arg842=
XM_011510792.1:c.3518G= XP_011509094.1:p.Arg1173=
XR_922888.1:n.3655G=
XM_011510778.3:c.3518G= XP_011509080.1:p.Arg1173=
XM_011510779.2:c.3518G= XP_011509081.1:p.Arg1173=
XM_011510780.2:c.3515G= XP_011509082.1:p.Arg1172=
XM_011510781.3:c.3500G= XP_011509083.1:p.Arg1167=
XM_011510782.3:c.3518G= XP_011509084.1:p.Arg1173=
XM_011510783.3:c.3350G= XP_011509085.1:p.Arg1117=
XM_011510784.2:c.3347G= XP_011509086.1:p.Arg1116=
XM_011510785.3:c.3332G= XP_011509087.1:p.Arg1111=
XM_011510786.3:c.3227G= XP_011509088.1:p.Arg1076=
XM_011510789.2:c.3041G= XP_011509091.1:p.Arg1014=
XM_011510792.3:c.3518G= XP_011509094.1:p.Arg1173=
XM_017003568.1:c.3464G= XP_016859057.1:p.Arg1155=
XM_017003569.1:c.3296G= XP_016859058.1:p.Arg1099=
XM_017003570.1:c.3023G= XP_016859059.1:p.Arg1008=
XM_017003571.1:c.2873G= XP_016859060.1:p.Arg958=
XM_017003572.1:c.2525G= XP_016859061.1:p.Arg842=
XM_017003573.1:c.2525G= XP_016859062.1:p.Arg842=
XM_017003574.1:c.2525G= XP_016859063.1:p.Arg842=
NM_015040.4:c.3482G= MANE Select NP_055855.2:p.Arg1161=