Canonical Allele Identifier: CA350115583

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209190990T>A (hg19) ; chr2:g.208326266T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326266T>A , CM000664.2:g.208326266T>A	GRCh38
NC_000002.11:g.209190990T>A , CM000664.1:g.209190990T>A	GRCh37
NC_000002.10:g.208899235T>A	NCBI36
NG_021188.1:g.65000T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3455T>A MANE Select	ENSP00000264380.4:p.Leu1152Gln
ENST00000264380.8:c.3455T>A	ENSP00000264380.4:p.Leu1152Gln
ENST00000452564.1:c.3287T>A	ENSP00000405736.1:p.Leu1096Gln
NM_015040.3:c.3455T>A	NP_055855.2:p.Leu1152Gln
XM_011510778.1:c.3491T>A	XP_011509080.1:p.Leu1164Gln
XM_011510779.1:c.3491T>A	XP_011509081.1:p.Leu1164Gln
XM_011510780.1:c.3488T>A	XP_011509082.1:p.Leu1163Gln
XM_011510781.1:c.3473T>A	XP_011509083.1:p.Leu1158Gln
XM_011510782.1:c.3491T>A	XP_011509084.1:p.Leu1164Gln
XM_011510783.1:c.3323T>A	XP_011509085.1:p.Leu1108Gln
XM_011510784.1:c.3320T>A	XP_011509086.1:p.Leu1107Gln
XM_011510785.1:c.3305T>A	XP_011509087.1:p.Leu1102Gln
XM_011510786.1:c.3200T>A	XP_011509088.1:p.Leu1067Gln
XM_011510787.1:c.3197T>A	XP_011509089.1:p.Leu1066Gln
XM_011510788.1:c.3164T>A	XP_011509090.1:p.Leu1055Gln
XM_011510789.1:c.3014T>A	XP_011509091.1:p.Leu1005Gln
XM_011510790.1:c.2498T>A	XP_011509092.1:p.Leu833Gln
XM_011510791.1:c.2498T>A	XP_011509093.1:p.Leu833Gln
XM_011510792.1:c.3491T>A	XP_011509094.1:p.Leu1164Gln
XR_922888.1:n.3628T>A
XM_011510778.3:c.3491T>A	XP_011509080.1:p.Leu1164Gln
XM_011510779.2:c.3491T>A	XP_011509081.1:p.Leu1164Gln
XM_011510780.2:c.3488T>A	XP_011509082.1:p.Leu1163Gln
XM_011510781.3:c.3473T>A	XP_011509083.1:p.Leu1158Gln
XM_011510782.3:c.3491T>A	XP_011509084.1:p.Leu1164Gln
XM_011510783.3:c.3323T>A	XP_011509085.1:p.Leu1108Gln
XM_011510784.2:c.3320T>A	XP_011509086.1:p.Leu1107Gln
XM_011510785.3:c.3305T>A	XP_011509087.1:p.Leu1102Gln
XM_011510786.3:c.3200T>A	XP_011509088.1:p.Leu1067Gln
XM_011510789.2:c.3014T>A	XP_011509091.1:p.Leu1005Gln
XM_011510792.3:c.3491T>A	XP_011509094.1:p.Leu1164Gln
XM_017003568.1:c.3437T>A	XP_016859057.1:p.Leu1146Gln
XM_017003569.1:c.3269T>A	XP_016859058.1:p.Leu1090Gln
XM_017003570.1:c.2996T>A	XP_016859059.1:p.Leu999Gln
XM_017003571.1:c.2846T>A	XP_016859060.1:p.Leu949Gln
XM_017003572.1:c.2498T>A	XP_016859061.1:p.Leu833Gln
XM_017003573.1:c.2498T>A	XP_016859062.1:p.Leu833Gln
XM_017003574.1:c.2498T>A	XP_016859063.1:p.Leu833Gln
NM_015040.4:c.3455T>A MANE Select	NP_055855.2:p.Leu1152Gln