Canonical Allele Identifier: CA1324023438
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326263T= , CM000664.2:g.208326263T= GRCh38
NC_000002.11:g.209190987T= , CM000664.1:g.209190987T= GRCh37
NC_000002.10:g.208899232T= NCBI36
NG_021188.1:g.64997T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3452T= MANE Select ENSP00000264380.4:p.Met1151=
ENST00000264380.8:c.3452T= ENSP00000264380.4:p.Met1151=
ENST00000452564.1:c.3284T= ENSP00000405736.1:p.Met1095=
NM_015040.3:c.3452T= NP_055855.2:p.Met1151=
XM_011510778.1:c.3488T= XP_011509080.1:p.Met1163=
XM_011510779.1:c.3488T= XP_011509081.1:p.Met1163=
XM_011510780.1:c.3485T= XP_011509082.1:p.Met1162=
XM_011510781.1:c.3470T= XP_011509083.1:p.Met1157=
XM_011510782.1:c.3488T= XP_011509084.1:p.Met1163=
XM_011510783.1:c.3320T= XP_011509085.1:p.Met1107=
XM_011510784.1:c.3317T= XP_011509086.1:p.Met1106=
XM_011510785.1:c.3302T= XP_011509087.1:p.Met1101=
XM_011510786.1:c.3197T= XP_011509088.1:p.Met1066=
XM_011510787.1:c.3194T= XP_011509089.1:p.Met1065=
XM_011510788.1:c.3161T= XP_011509090.1:p.Met1054=
XM_011510789.1:c.3011T= XP_011509091.1:p.Met1004=
XM_011510790.1:c.2495T= XP_011509092.1:p.Met832=
XM_011510791.1:c.2495T= XP_011509093.1:p.Met832=
XM_011510792.1:c.3488T= XP_011509094.1:p.Met1163=
XR_922888.1:n.3625T=
XM_011510778.3:c.3488T= XP_011509080.1:p.Met1163=
XM_011510779.2:c.3488T= XP_011509081.1:p.Met1163=
XM_011510780.2:c.3485T= XP_011509082.1:p.Met1162=
XM_011510781.3:c.3470T= XP_011509083.1:p.Met1157=
XM_011510782.3:c.3488T= XP_011509084.1:p.Met1163=
XM_011510783.3:c.3320T= XP_011509085.1:p.Met1107=
XM_011510784.2:c.3317T= XP_011509086.1:p.Met1106=
XM_011510785.3:c.3302T= XP_011509087.1:p.Met1101=
XM_011510786.3:c.3197T= XP_011509088.1:p.Met1066=
XM_011510789.2:c.3011T= XP_011509091.1:p.Met1004=
XM_011510792.3:c.3488T= XP_011509094.1:p.Met1163=
XM_017003568.1:c.3434T= XP_016859057.1:p.Met1145=
XM_017003569.1:c.3266T= XP_016859058.1:p.Met1089=
XM_017003570.1:c.2993T= XP_016859059.1:p.Met998=
XM_017003571.1:c.2843T= XP_016859060.1:p.Met948=
XM_017003572.1:c.2495T= XP_016859061.1:p.Met832=
XM_017003573.1:c.2495T= XP_016859062.1:p.Met832=
XM_017003574.1:c.2495T= XP_016859063.1:p.Met832=
NM_015040.4:c.3452T= MANE Select NP_055855.2:p.Met1151=