Canonical Allele Identifier: CA390160033

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67754213C>T , CM000676.2:g.67754213C>T	GRCh38
NC_000014.8:g.68220930C>T , CM000676.1:g.68220930C>T	GRCh37
NC_000014.7:g.67290683C>T	NCBI36
NG_011836.1:g.67377G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.6987-1G>A MANE Select	NP_056161.2:n.6987-1G>A
ENST00000347230.9:c.6987-1G>A MANE Select	ENSP00000251119.5:n.6987-1G>A
NM_015346.3:c.6987-1G>A	NP_056161.2:n.6987-1G>A
ENST00000347230.8:c.6987-1G>A	ENSP00000251119.5:n.6987-1G>A
ENST00000394455.6:n.2250-1G>A
ENST00000554523.5:n.7742-1G>A
ENST00000554557.5:c.*4965-1G>A	ENSP00000450431.1:n.*4965-1G>A
ENST00000554783.1:n.675-1G>A
ENST00000557306.1:c.525-1G>A	ENSP00000452142.1:n.525-1G>A
ENST00000676512.1:c.7005-1G>A	ENSP00000504552.1:n.7005-1G>A
ENST00000676620.1:c.6909-1G>A	ENSP00000504587.1:n.6909-1G>A
ENST00000678386.1:c.7032-1G>A	ENSP00000503677.1:n.7032-1G>A
XM_006720093.2:c.6987-1G>A	XP_006720156.1:n.6987-1G>A
XM_011536606.1:c.5478-1G>A	XP_011534908.1:n.5478-1G>A
XM_011536607.1:c.4662-1G>A	XP_011534909.1:n.4662-1G>A
XM_011536608.1:c.4569-1G>A	XP_011534910.1:n.4569-1G>A
XM_017021124.1:c.7005-1G>A	XP_016876613.1:n.7005-1G>A
XM_017021125.1:c.7005-1G>A	XP_016876614.1:n.7005-1G>A
XM_017021126.1:c.5496-1G>A	XP_016876615.1:n.5496-1G>A
XM_017021127.2:c.4680-1G>A	XP_016876616.1:n.4680-1G>A
XM_017021128.1:c.4587-1G>A	XP_016876617.1:n.4587-1G>A