Canonical Allele Identifier: CA2580088643

Gene: ZFYVE26

Linked Data

• ClinVar Variation Id: 1726492
• ClinVar RCV Id: RCV002310176

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67782869_67782870delinsA , CM000676.2:g.67782869_67782870delinsA	GRCh38
NC_000014.8:g.68249586_68249587delinsA , CM000676.1:g.68249586_68249587delinsA	GRCh37
NC_000014.7:g.67319339_67319340delinsA	NCBI36
NG_011836.1:g.38720_38721delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4282_4283delinsT MANE Select	ENSP00000251119.5:p.Arg1428TrpfsTer16
ENST00000676512.1:c.4282_4283delinsT	ENSP00000504552.1:p.Arg1428TrpfsTer16
ENST00000676620.1:c.4282_4283delinsT	ENSP00000504587.1:p.Arg1428TrpfsTer16
ENST00000678386.1:c.4282_4283delinsT	ENSP00000503677.1:p.Arg1428TrpfsTer16
ENST00000347230.8:c.4282_4283delinsT	ENSP00000251119.5:p.Arg1428TrpfsTer16
ENST00000554523.5:n.4419_4420delinsT
ENST00000554557.5:c.*2350+229_*2350+230delinsT	ENSP00000450431.1:n.*2350+229_*2350+230delinsT
ENST00000555452.1:c.4282_4283delinsT	ENSP00000450603.1:p.Arg1428TrpfsTer16
NM_015346.3:c.4282_4283delinsT	NP_056161.2:p.Arg1428TrpfsTer16
XM_006720093.2:c.4282_4283delinsT	XP_006720156.1:p.Arg1428TrpfsTer16
XM_011536606.1:c.2773_2774delinsT	XP_011534908.1:p.Arg925TrpfsTer16
XM_011536607.1:c.1957_1958delinsT	XP_011534909.1:p.Arg653TrpfsTer16
XM_011536608.1:c.1864_1865delinsT	XP_011534910.1:p.Arg622TrpfsTer16
XM_011536609.1:c.4282_4283delinsT	XP_011534911.1:p.Arg1428TrpfsTer16
XM_011536609.2:c.4282_4283delinsT	XP_011534911.1:p.Arg1428TrpfsTer16
XM_017021124.1:c.4282_4283delinsT	XP_016876613.1:p.Arg1428TrpfsTer16
XM_017021125.1:c.4282_4283delinsT	XP_016876614.1:p.Arg1428TrpfsTer16
XM_017021126.1:c.2773_2774delinsT	XP_016876615.1:p.Arg925TrpfsTer16
XM_017021127.2:c.1957_1958delinsT	XP_016876616.1:p.Arg653TrpfsTer16
XM_017021128.1:c.1864_1865delinsT	XP_016876617.1:p.Arg622TrpfsTer16
NM_015346.4:c.4282_4283delinsT MANE Select	NP_056161.2:p.Arg1428TrpfsTer16