Canonical Allele Identifier: CA7240401

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67798165G>T , CM000676.2:g.67798165G>T	GRCh38
NC_000014.8:g.68264882G>T , CM000676.1:g.68264882G>T	GRCh37
NC_000014.7:g.67334635G>T	NCBI36
NG_011836.1:g.23425C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.2097C>A MANE Select	NP_056161.2:p.Ile699=
ENST00000347230.9:c.2097C>A MANE Select	ENSP00000251119.5:p.Ile699=
NM_015346.3:c.2097C>A	NP_056161.2:p.Ile699=
ENST00000347230.8:c.2097C>A	ENSP00000251119.5:p.Ile699=
ENST00000554523.5:n.2234C>A
ENST00000554557.5:c.*394C>A	ENSP00000450431.1:n.*394C>A
ENST00000555452.1:c.2097C>A	ENSP00000450603.1:p.Ile699=
ENST00000557366.5:n.2143C>A
ENST00000557407.1:n.2232C>A
ENST00000676512.1:c.2097C>A	ENSP00000504552.1:p.Ile699=
ENST00000676620.1:c.2097C>A	ENSP00000504587.1:p.Ile699=
ENST00000677026.1:c.1893C>A	ENSP00000503710.1:p.Ile631=
ENST00000678382.1:c.*1092C>A	ENSP00000504130.1:n.*1092C>A
ENST00000678386.1:c.2097C>A	ENSP00000503677.1:p.Ile699=
XM_006720093.2:c.2097C>A	XP_006720156.1:p.Ile699=
XM_011536606.1:c.588C>A	XP_011534908.1:p.Ile196=
XM_011536609.1:c.2097C>A	XP_011534911.1:p.Ile699=
XM_011536609.2:c.2097C>A	XP_011534911.1:p.Ile699=
XM_017021124.1:c.2097C>A	XP_016876613.1:p.Ile699=
XM_017021125.1:c.2097C>A	XP_016876614.1:p.Ile699=
XM_017021126.1:c.588C>A	XP_016876615.1:p.Ile196=