Canonical Allele Identifier: CA350115695

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209191044T>C (hg19) ; chr2:g.208326320T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326320T>C , CM000664.2:g.208326320T>C	GRCh38
NC_000002.11:g.209191044T>C , CM000664.1:g.209191044T>C	GRCh37
NC_000002.10:g.208899289T>C	NCBI36
NG_021188.1:g.65054T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3509T>C MANE Select	ENSP00000264380.4:p.Phe1170Ser
ENST00000264380.8:c.3509T>C	ENSP00000264380.4:p.Phe1170Ser
ENST00000452564.1:c.3341T>C	ENSP00000405736.1:p.Phe1114Ser
NM_015040.3:c.3509T>C	NP_055855.2:p.Phe1170Ser
XM_011510778.1:c.3545T>C	XP_011509080.1:p.Phe1182Ser
XM_011510779.1:c.3545T>C	XP_011509081.1:p.Phe1182Ser
XM_011510780.1:c.3542T>C	XP_011509082.1:p.Phe1181Ser
XM_011510781.1:c.3527T>C	XP_011509083.1:p.Phe1176Ser
XM_011510782.1:c.3545T>C	XP_011509084.1:p.Phe1182Ser
XM_011510783.1:c.3377T>C	XP_011509085.1:p.Phe1126Ser
XM_011510784.1:c.3374T>C	XP_011509086.1:p.Phe1125Ser
XM_011510785.1:c.3359T>C	XP_011509087.1:p.Phe1120Ser
XM_011510786.1:c.3254T>C	XP_011509088.1:p.Phe1085Ser
XM_011510787.1:c.3251T>C	XP_011509089.1:p.Phe1084Ser
XM_011510788.1:c.3218T>C	XP_011509090.1:p.Phe1073Ser
XM_011510789.1:c.3068T>C	XP_011509091.1:p.Phe1023Ser
XM_011510790.1:c.2552T>C	XP_011509092.1:p.Phe851Ser
XM_011510791.1:c.2552T>C	XP_011509093.1:p.Phe851Ser
XM_011510792.1:c.3545T>C	XP_011509094.1:p.Phe1182Ser
XR_922888.1:n.3682T>C
XM_011510778.3:c.3545T>C	XP_011509080.1:p.Phe1182Ser
XM_011510779.2:c.3545T>C	XP_011509081.1:p.Phe1182Ser
XM_011510780.2:c.3542T>C	XP_011509082.1:p.Phe1181Ser
XM_011510781.3:c.3527T>C	XP_011509083.1:p.Phe1176Ser
XM_011510782.3:c.3545T>C	XP_011509084.1:p.Phe1182Ser
XM_011510783.3:c.3377T>C	XP_011509085.1:p.Phe1126Ser
XM_011510784.2:c.3374T>C	XP_011509086.1:p.Phe1125Ser
XM_011510785.3:c.3359T>C	XP_011509087.1:p.Phe1120Ser
XM_011510786.3:c.3254T>C	XP_011509088.1:p.Phe1085Ser
XM_011510789.2:c.3068T>C	XP_011509091.1:p.Phe1023Ser
XM_011510792.3:c.3545T>C	XP_011509094.1:p.Phe1182Ser
XM_017003568.1:c.3491T>C	XP_016859057.1:p.Phe1164Ser
XM_017003569.1:c.3323T>C	XP_016859058.1:p.Phe1108Ser
XM_017003570.1:c.3050T>C	XP_016859059.1:p.Phe1017Ser
XM_017003571.1:c.2900T>C	XP_016859060.1:p.Phe967Ser
XM_017003572.1:c.2552T>C	XP_016859061.1:p.Phe851Ser
XM_017003573.1:c.2552T>C	XP_016859062.1:p.Phe851Ser
XM_017003574.1:c.2552T>C	XP_016859063.1:p.Phe851Ser
NM_015040.4:c.3509T>C MANE Select	NP_055855.2:p.Phe1170Ser