Canonical Allele Identifier: CA7240431

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67798392C>T , CM000676.2:g.67798392C>T	GRCh38
NC_000014.8:g.68265109C>T , CM000676.1:g.68265109C>T	GRCh37
NC_000014.7:g.67334862C>T	NCBI36
NG_011836.1:g.23198G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.1870G>A MANE Select	NP_056161.2:p.Ala624Thr
ENST00000347230.9:c.1870G>A MANE Select	ENSP00000251119.5:p.Ala624Thr
NM_015346.3:c.1870G>A	NP_056161.2:p.Ala624Thr
ENST00000347230.8:c.1870G>A	ENSP00000251119.5:p.Ala624Thr
ENST00000554523.5:n.2007G>A
ENST00000554557.5:c.*167G>A	ENSP00000450431.1:n.*167G>A
ENST00000555452.1:c.1870G>A	ENSP00000450603.1:p.Ala624Thr
ENST00000557366.5:n.1916G>A
ENST00000557407.1:n.2005G>A
ENST00000676512.1:c.1870G>A	ENSP00000504552.1:p.Ala624Thr
ENST00000676620.1:c.1870G>A	ENSP00000504587.1:p.Ala624Thr
ENST00000677026.1:c.1666G>A	ENSP00000503710.1:p.Ala556Thr
ENST00000678382.1:c.*865G>A	ENSP00000504130.1:n.*865G>A
ENST00000678386.1:c.1870G>A	ENSP00000503677.1:p.Ala624Thr
XM_006720093.2:c.1870G>A	XP_006720156.1:p.Ala624Thr
XM_011536606.1:c.361G>A	XP_011534908.1:p.Ala121Thr
XM_011536609.1:c.1870G>A	XP_011534911.1:p.Ala624Thr
XM_011536609.2:c.1870G>A	XP_011534911.1:p.Ala624Thr
XM_017021124.1:c.1870G>A	XP_016876613.1:p.Ala624Thr
XM_017021125.1:c.1870G>A	XP_016876614.1:p.Ala624Thr
XM_017021126.1:c.361G>A	XP_016876615.1:p.Ala121Thr