Canonical Allele Identifier: CA262812942

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67754069A>T , CM000676.2:g.67754069A>T	GRCh38
NC_000014.8:g.68220786A>T , CM000676.1:g.68220786A>T	GRCh37
NC_000014.7:g.67290539A>T	NCBI36
NG_011836.1:g.67521T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.7128+2T>A MANE Select	NP_056161.2:n.7128+2T>A
ENST00000347230.9:c.7128+2T>A MANE Select	ENSP00000251119.5:n.7128+2T>A
NM_015346.3:c.7128+2T>A	NP_056161.2:n.7128+2T>A
ENST00000347230.8:c.7128+2T>A	ENSP00000251119.5:n.7128+2T>A
ENST00000394455.6:n.2391+2T>A
ENST00000554523.5:n.7883+2T>A
ENST00000554557.5:c.*5106+2T>A	ENSP00000450431.1:n.*5106+2T>A
ENST00000554783.1:n.816+2T>A
ENST00000557306.1:c.666+2T>A	ENSP00000452142.1:n.666+2T>A
ENST00000676512.1:c.7146+2T>A	ENSP00000504552.1:n.7146+2T>A
ENST00000676620.1:c.7050+2T>A	ENSP00000504587.1:n.7050+2T>A
ENST00000678386.1:c.7173+2T>A	ENSP00000503677.1:n.7173+2T>A
XM_006720093.2:c.7128+2T>A	XP_006720156.1:n.7128+2T>A
XM_011536606.1:c.5619+2T>A	XP_011534908.1:n.5619+2T>A
XM_011536607.1:c.4803+2T>A	XP_011534909.1:n.4803+2T>A
XM_011536608.1:c.4710+2T>A	XP_011534910.1:n.4710+2T>A
XM_017021124.1:c.7146+2T>A	XP_016876613.1:n.7146+2T>A
XM_017021125.1:c.7146+2T>A	XP_016876614.1:n.7146+2T>A
XM_017021126.1:c.5637+2T>A	XP_016876615.1:n.5637+2T>A
XM_017021127.2:c.4821+2T>A	XP_016876616.1:n.4821+2T>A
XM_017021128.1:c.4728+2T>A	XP_016876617.1:n.4728+2T>A