Canonical Allele Identifier: CA7240304

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67794176G>A , CM000676.2:g.67794176G>A	GRCh38
NC_000014.8:g.68260893G>A , CM000676.1:g.68260893G>A	GRCh37
NC_000014.7:g.67330646G>A	NCBI36
NG_011836.1:g.27414C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.2396C>T MANE Select	NP_056161.2:p.Thr799Met
ENST00000347230.9:c.2396C>T MANE Select	ENSP00000251119.5:p.Thr799Met
NM_015346.3:c.2396C>T	NP_056161.2:p.Thr799Met
ENST00000347230.8:c.2396C>T	ENSP00000251119.5:p.Thr799Met
ENST00000554523.5:n.2533C>T
ENST00000554557.5:c.*693C>T	ENSP00000450431.1:n.*693C>T
ENST00000555452.1:c.2396C>T	ENSP00000450603.1:p.Thr799Met
ENST00000676512.1:c.2396C>T	ENSP00000504552.1:p.Thr799Met
ENST00000676620.1:c.2396C>T	ENSP00000504587.1:p.Thr799Met
ENST00000677026.1:c.2192C>T	ENSP00000503710.1:p.Thr731Met
ENST00000678382.1:c.*1391C>T	ENSP00000504130.1:n.*1391C>T
ENST00000678386.1:c.2396C>T	ENSP00000503677.1:p.Thr799Met
XM_006720093.2:c.2396C>T	XP_006720156.1:p.Thr799Met
XM_011536606.1:c.887C>T	XP_011534908.1:p.Thr296Met
XM_011536607.1:c.71C>T	XP_011534909.1:p.Thr24Met
XM_011536608.1:c.-23C>T	XP_011534910.1:n.-23C>T
XM_011536609.1:c.2396C>T	XP_011534911.1:p.Thr799Met
XM_011536609.2:c.2396C>T	XP_011534911.1:p.Thr799Met
XM_017021124.1:c.2396C>T	XP_016876613.1:p.Thr799Met
XM_017021125.1:c.2396C>T	XP_016876614.1:p.Thr799Met
XM_017021126.1:c.887C>T	XP_016876615.1:p.Thr296Met
XM_017021127.2:c.71C>T	XP_016876616.1:p.Thr24Met
XM_017021128.1:c.-23C>T	XP_016876617.1:n.-23C>T