Canonical Allele Identifier: CA350115644

Gene: PIKFYVE

Linked Data

• MyVariant Identifiers: chr2:g.209191020T>G (hg19) ; chr2:g.208326296T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326296T>G , CM000664.2:g.208326296T>G	GRCh38
NC_000002.11:g.209191020T>G , CM000664.1:g.209191020T>G	GRCh37
NC_000002.10:g.208899265T>G	NCBI36
NG_021188.1:g.65030T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3485T>G MANE Select	ENSP00000264380.4:p.Ile1162Ser
ENST00000264380.8:c.3485T>G	ENSP00000264380.4:p.Ile1162Ser
ENST00000452564.1:c.3317T>G	ENSP00000405736.1:p.Ile1106Ser
NM_015040.3:c.3485T>G	NP_055855.2:p.Ile1162Ser
XM_011510778.1:c.3521T>G	XP_011509080.1:p.Ile1174Ser
XM_011510779.1:c.3521T>G	XP_011509081.1:p.Ile1174Ser
XM_011510780.1:c.3518T>G	XP_011509082.1:p.Ile1173Ser
XM_011510781.1:c.3503T>G	XP_011509083.1:p.Ile1168Ser
XM_011510782.1:c.3521T>G	XP_011509084.1:p.Ile1174Ser
XM_011510783.1:c.3353T>G	XP_011509085.1:p.Ile1118Ser
XM_011510784.1:c.3350T>G	XP_011509086.1:p.Ile1117Ser
XM_011510785.1:c.3335T>G	XP_011509087.1:p.Ile1112Ser
XM_011510786.1:c.3230T>G	XP_011509088.1:p.Ile1077Ser
XM_011510787.1:c.3227T>G	XP_011509089.1:p.Ile1076Ser
XM_011510788.1:c.3194T>G	XP_011509090.1:p.Ile1065Ser
XM_011510789.1:c.3044T>G	XP_011509091.1:p.Ile1015Ser
XM_011510790.1:c.2528T>G	XP_011509092.1:p.Ile843Ser
XM_011510791.1:c.2528T>G	XP_011509093.1:p.Ile843Ser
XM_011510792.1:c.3521T>G	XP_011509094.1:p.Ile1174Ser
XR_922888.1:n.3658T>G
XM_011510778.3:c.3521T>G	XP_011509080.1:p.Ile1174Ser
XM_011510779.2:c.3521T>G	XP_011509081.1:p.Ile1174Ser
XM_011510780.2:c.3518T>G	XP_011509082.1:p.Ile1173Ser
XM_011510781.3:c.3503T>G	XP_011509083.1:p.Ile1168Ser
XM_011510782.3:c.3521T>G	XP_011509084.1:p.Ile1174Ser
XM_011510783.3:c.3353T>G	XP_011509085.1:p.Ile1118Ser
XM_011510784.2:c.3350T>G	XP_011509086.1:p.Ile1117Ser
XM_011510785.3:c.3335T>G	XP_011509087.1:p.Ile1112Ser
XM_011510786.3:c.3230T>G	XP_011509088.1:p.Ile1077Ser
XM_011510789.2:c.3044T>G	XP_011509091.1:p.Ile1015Ser
XM_011510792.3:c.3521T>G	XP_011509094.1:p.Ile1174Ser
XM_017003568.1:c.3467T>G	XP_016859057.1:p.Ile1156Ser
XM_017003569.1:c.3299T>G	XP_016859058.1:p.Ile1100Ser
XM_017003570.1:c.3026T>G	XP_016859059.1:p.Ile1009Ser
XM_017003571.1:c.2876T>G	XP_016859060.1:p.Ile959Ser
XM_017003572.1:c.2528T>G	XP_016859061.1:p.Ile843Ser
XM_017003573.1:c.2528T>G	XP_016859062.1:p.Ile843Ser
XM_017003574.1:c.2528T>G	XP_016859063.1:p.Ile843Ser
NM_015040.4:c.3485T>G MANE Select	NP_055855.2:p.Ile1162Ser