Canonical Allele Identifier: CA390162082

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67756147T>C , CM000676.2:g.67756147T>C	GRCh38
NC_000014.8:g.68222864T>C , CM000676.1:g.68222864T>C	GRCh37
NC_000014.7:g.67292617T>C	NCBI36
NG_011836.1:g.65443A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.6589-2A>G MANE Select	NP_056161.2:n.6589-2A>G
ENST00000347230.9:c.6589-2A>G MANE Select	ENSP00000251119.5:n.6589-2A>G
NM_015346.3:c.6589-2A>G	NP_056161.2:n.6589-2A>G
ENST00000347230.8:c.6589-2A>G	ENSP00000251119.5:n.6589-2A>G
ENST00000394455.6:n.1852-2A>G
ENST00000554523.5:n.7344-2A>G
ENST00000554557.5:c.*4567-2A>G	ENSP00000450431.1:n.*4567-2A>G
ENST00000554783.1:n.275A>G
ENST00000557306.1:c.127-2A>G	ENSP00000452142.1:n.127-2A>G
ENST00000676512.1:c.6607-2A>G	ENSP00000504552.1:n.6607-2A>G
ENST00000676620.1:c.6511-2A>G	ENSP00000504587.1:n.6511-2A>G
ENST00000678386.1:c.6634-2A>G	ENSP00000503677.1:n.6634-2A>G
XM_006720093.2:c.6589-2A>G	XP_006720156.1:n.6589-2A>G
XM_011536606.1:c.5080-2A>G	XP_011534908.1:n.5080-2A>G
XM_011536607.1:c.4264-2A>G	XP_011534909.1:n.4264-2A>G
XM_011536608.1:c.4171-2A>G	XP_011534910.1:n.4171-2A>G
XM_017021124.1:c.6607-2A>G	XP_016876613.1:n.6607-2A>G
XM_017021125.1:c.6607-2A>G	XP_016876614.1:n.6607-2A>G
XM_017021126.1:c.5098-2A>G	XP_016876615.1:n.5098-2A>G
XM_017021127.2:c.4282-2A>G	XP_016876616.1:n.4282-2A>G
XM_017021128.1:c.4189-2A>G	XP_016876617.1:n.4189-2A>G