Canonical Allele Identifier: CA486762560

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67755140C>T , CM000676.2:g.67755140C>T	GRCh38
NC_000014.8:g.68221857C>T , CM000676.1:g.68221857C>T	GRCh37
NC_000014.7:g.67291610C>T	NCBI36
NG_011836.1:g.66450G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.6897G>A MANE Select	NP_056161.2:p.Leu2299=
ENST00000347230.9:c.6897G>A MANE Select	ENSP00000251119.5:p.Leu2299=
NM_015346.3:c.6897G>A	NP_056161.2:p.Leu2299=
ENST00000347230.8:c.6897G>A	ENSP00000251119.5:p.Leu2299=
ENST00000394455.6:n.2160G>A
ENST00000554523.5:n.7652G>A
ENST00000554557.5:c.*4875G>A	ENSP00000450431.1:n.*4875G>A
ENST00000554783.1:n.585G>A
ENST00000557306.1:c.435G>A	ENSP00000452142.1:p.Leu145=
ENST00000676512.1:c.6915G>A	ENSP00000504552.1:p.Leu2305=
ENST00000676620.1:c.6819G>A	ENSP00000504587.1:p.Leu2273=
ENST00000678386.1:c.6942G>A	ENSP00000503677.1:p.Leu2314=
XM_006720093.2:c.6897G>A	XP_006720156.1:p.Leu2299=
XM_011536606.1:c.5388G>A	XP_011534908.1:p.Leu1796=
XM_011536607.1:c.4572G>A	XP_011534909.1:p.Leu1524=
XM_011536608.1:c.4479G>A	XP_011534910.1:p.Leu1493=
XM_017021124.1:c.6915G>A	XP_016876613.1:p.Leu2305=
XM_017021125.1:c.6915G>A	XP_016876614.1:p.Leu2305=
XM_017021126.1:c.5406G>A	XP_016876615.1:p.Leu1802=
XM_017021127.2:c.4590G>A	XP_016876616.1:p.Leu1530=
XM_017021128.1:c.4497G>A	XP_016876617.1:p.Leu1499=