Canonical Allele Identifier: CA390166565

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67767804G>T , CM000676.2:g.67767804G>T	GRCh38
NC_000014.8:g.68234521G>T , CM000676.1:g.68234521G>T	GRCh37
NC_000014.7:g.67304274G>T	NCBI36
NG_011836.1:g.53786C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.5690C>A MANE Select	NP_056161.2:p.Ser1897Ter
ENST00000347230.9:c.5690C>A MANE Select	ENSP00000251119.5:p.Ser1897Ter
NM_015346.3:c.5690C>A	NP_056161.2:p.Ser1897Ter
ENST00000347230.8:c.5690C>A	ENSP00000251119.5:p.Ser1897Ter
ENST00000394455.6:n.953C>A
ENST00000554523.5:n.5827C>A
ENST00000554557.5:c.*3668C>A	ENSP00000450431.1:n.*3668C>A
ENST00000555452.1:c.5690C>A	ENSP00000450603.1:p.Ser1897Ter
ENST00000676512.1:c.5708C>A	ENSP00000504552.1:p.Ser1903Ter
ENST00000676620.1:c.5612C>A	ENSP00000504587.1:p.Ser1871Ter
ENST00000678386.1:c.5735C>A	ENSP00000503677.1:p.Ser1912Ter
XM_006720093.2:c.5690C>A	XP_006720156.1:p.Ser1897Ter
XM_011536606.1:c.4181C>A	XP_011534908.1:p.Ser1394Ter
XM_011536607.1:c.3365C>A	XP_011534909.1:p.Ser1122Ter
XM_011536608.1:c.3272C>A	XP_011534910.1:p.Ser1091Ter
XM_017021124.1:c.5708C>A	XP_016876613.1:p.Ser1903Ter
XM_017021125.1:c.5708C>A	XP_016876614.1:p.Ser1903Ter
XM_017021126.1:c.4199C>A	XP_016876615.1:p.Ser1400Ter
XM_017021127.2:c.3383C>A	XP_016876616.1:p.Ser1128Ter
XM_017021128.1:c.3290C>A	XP_016876617.1:p.Ser1097Ter