Canonical Allele Identifier: CA390163765

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67762241C>A , CM000676.2:g.67762241C>A	GRCh38
NC_000014.8:g.68228958C>A , CM000676.1:g.68228958C>A	GRCh37
NC_000014.7:g.67298711C>A	NCBI36
NG_011836.1:g.59349G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.6331G>T MANE Select	NP_056161.2:p.Glu2111Ter
ENST00000347230.9:c.6331G>T MANE Select	ENSP00000251119.5:p.Glu2111Ter
NM_015346.3:c.6331G>T	NP_056161.2:p.Glu2111Ter
ENST00000347230.8:c.6331G>T	ENSP00000251119.5:p.Glu2111Ter
ENST00000394455.6:n.1594G>T
ENST00000554523.5:n.6468G>T
ENST00000554557.5:c.*4309G>T	ENSP00000450431.1:n.*4309G>T
ENST00000555452.1:c.6331G>T	ENSP00000450603.1:p.Glu2111Ter
ENST00000676512.1:c.6349G>T	ENSP00000504552.1:p.Glu2117Ter
ENST00000676620.1:c.6253G>T	ENSP00000504587.1:p.Glu2085Ter
ENST00000678386.1:c.6376G>T	ENSP00000503677.1:p.Glu2126Ter
XM_006720093.2:c.6331G>T	XP_006720156.1:p.Glu2111Ter
XM_011536606.1:c.4822G>T	XP_011534908.1:p.Glu1608Ter
XM_011536607.1:c.4006G>T	XP_011534909.1:p.Glu1336Ter
XM_011536608.1:c.3913G>T	XP_011534910.1:p.Glu1305Ter
XM_017021124.1:c.6349G>T	XP_016876613.1:p.Glu2117Ter
XM_017021125.1:c.6349G>T	XP_016876614.1:p.Glu2117Ter
XM_017021126.1:c.4840G>T	XP_016876615.1:p.Glu1614Ter
XM_017021127.2:c.4024G>T	XP_016876616.1:p.Glu1342Ter
XM_017021128.1:c.3931G>T	XP_016876617.1:p.Glu1311Ter