Canonical Allele Identifier: CA431117655
Gene: PIKFYVE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.209190931G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326207G>A , CM000664.2:g.208326207G>A GRCh38
NC_000002.11:g.209190931G>A , CM000664.1:g.209190931G>A GRCh37
NC_000002.10:g.208899176G>A NCBI36
NG_021188.1:g.64941G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3396G>A MANE Select ENSP00000264380.4:p.Glu1132=
ENST00000264380.8:c.3396G>A ENSP00000264380.4:p.Glu1132=
ENST00000452564.1:c.3228G>A ENSP00000405736.1:p.Glu1076=
NM_015040.3:c.3396G>A NP_055855.2:p.Glu1132=
XM_011510778.1:c.3432G>A XP_011509080.1:p.Glu1144=
XM_011510779.1:c.3432G>A XP_011509081.1:p.Glu1144=
XM_011510780.1:c.3429G>A XP_011509082.1:p.Glu1143=
XM_011510781.1:c.3414G>A XP_011509083.1:p.Glu1138=
XM_011510782.1:c.3432G>A XP_011509084.1:p.Glu1144=
XM_011510783.1:c.3264G>A XP_011509085.1:p.Glu1088=
XM_011510784.1:c.3261G>A XP_011509086.1:p.Glu1087=
XM_011510785.1:c.3246G>A XP_011509087.1:p.Glu1082=
XM_011510786.1:c.3141G>A XP_011509088.1:p.Glu1047=
XM_011510787.1:c.3138G>A XP_011509089.1:p.Glu1046=
XM_011510788.1:c.3105G>A XP_011509090.1:p.Glu1035=
XM_011510789.1:c.2955G>A XP_011509091.1:p.Glu985=
XM_011510790.1:c.2439G>A XP_011509092.1:p.Glu813=
XM_011510791.1:c.2439G>A XP_011509093.1:p.Glu813=
XM_011510792.1:c.3432G>A XP_011509094.1:p.Glu1144=
XR_922888.1:n.3569G>A
XM_011510778.3:c.3432G>A XP_011509080.1:p.Glu1144=
XM_011510779.2:c.3432G>A XP_011509081.1:p.Glu1144=
XM_011510780.2:c.3429G>A XP_011509082.1:p.Glu1143=
XM_011510781.3:c.3414G>A XP_011509083.1:p.Glu1138=
XM_011510782.3:c.3432G>A XP_011509084.1:p.Glu1144=
XM_011510783.3:c.3264G>A XP_011509085.1:p.Glu1088=
XM_011510784.2:c.3261G>A XP_011509086.1:p.Glu1087=
XM_011510785.3:c.3246G>A XP_011509087.1:p.Glu1082=
XM_011510786.3:c.3141G>A XP_011509088.1:p.Glu1047=
XM_011510789.2:c.2955G>A XP_011509091.1:p.Glu985=
XM_011510792.3:c.3432G>A XP_011509094.1:p.Glu1144=
XM_017003568.1:c.3378G>A XP_016859057.1:p.Glu1126=
XM_017003569.1:c.3210G>A XP_016859058.1:p.Glu1070=
XM_017003570.1:c.2937G>A XP_016859059.1:p.Glu979=
XM_017003571.1:c.2787G>A XP_016859060.1:p.Glu929=
XM_017003572.1:c.2439G>A XP_016859061.1:p.Glu813=
XM_017003573.1:c.2439G>A XP_016859062.1:p.Glu813=
XM_017003574.1:c.2439G>A XP_016859063.1:p.Glu813=
NM_015040.4:c.3396G>A MANE Select NP_055855.2:p.Glu1132=