Canonical Allele Identifier: CA390167019

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67769647G>T , CM000676.2:g.67769647G>T	GRCh38
NC_000014.8:g.68236364G>T , CM000676.1:g.68236364G>T	GRCh37
NC_000014.7:g.67306117G>T	NCBI36
NG_011836.1:g.51943C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.5568C>A MANE Select	NP_056161.2:p.Cys1856Ter
ENST00000347230.9:c.5568C>A MANE Select	ENSP00000251119.5:p.Cys1856Ter
NM_015346.3:c.5568C>A	NP_056161.2:p.Cys1856Ter
ENST00000347230.8:c.5568C>A	ENSP00000251119.5:p.Cys1856Ter
ENST00000394455.6:n.831C>A
ENST00000554523.5:n.5705C>A
ENST00000554557.5:c.*3546C>A	ENSP00000450431.1:n.*3546C>A
ENST00000555452.1:c.5568C>A	ENSP00000450603.1:p.Cys1856Ter
ENST00000676512.1:c.5586C>A	ENSP00000504552.1:p.Cys1862Ter
ENST00000676620.1:c.5490C>A	ENSP00000504587.1:p.Cys1830Ter
ENST00000678386.1:c.5613C>A	ENSP00000503677.1:p.Cys1871Ter
XM_006720093.2:c.5568C>A	XP_006720156.1:p.Cys1856Ter
XM_011536606.1:c.4059C>A	XP_011534908.1:p.Cys1353Ter
XM_011536607.1:c.3243C>A	XP_011534909.1:p.Cys1081Ter
XM_011536608.1:c.3150C>A	XP_011534910.1:p.Cys1050Ter
XM_017021124.1:c.5586C>A	XP_016876613.1:p.Cys1862Ter
XM_017021125.1:c.5586C>A	XP_016876614.1:p.Cys1862Ter
XM_017021126.1:c.4077C>A	XP_016876615.1:p.Cys1359Ter
XM_017021127.2:c.3261C>A	XP_016876616.1:p.Cys1087Ter
XM_017021128.1:c.3168C>A	XP_016876617.1:p.Cys1056Ter