Canonical Allele Identifier: CA7239523

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67772213G>A , CM000676.2:g.67772213G>A	GRCh38
NC_000014.8:g.68238930G>A , CM000676.1:g.68238930G>A	GRCh37
NC_000014.7:g.67308683G>A	NCBI36
NG_011836.1:g.49377C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.5321-3C>T MANE Select	NP_056161.2:n.5321-3C>T
ENST00000347230.9:c.5321-3C>T MANE Select	ENSP00000251119.5:n.5321-3C>T
NM_015346.3:c.5321-3C>T	NP_056161.2:n.5321-3C>T
ENST00000347230.8:c.5321-3C>T	ENSP00000251119.5:n.5321-3C>T
ENST00000554523.5:n.5458-3C>T
ENST00000554557.5:c.*3299-3C>T	ENSP00000450431.1:n.*3299-3C>T
ENST00000555452.1:c.5321-3C>T	ENSP00000450603.1:n.5321-3C>T
ENST00000676512.1:c.5339-3C>T	ENSP00000504552.1:n.5339-3C>T
ENST00000676620.1:c.5243-3C>T	ENSP00000504587.1:n.5243-3C>T
ENST00000678386.1:c.5366-3C>T	ENSP00000503677.1:n.5366-3C>T
XM_006720093.2:c.5321-3C>T	XP_006720156.1:n.5321-3C>T
XM_011536606.1:c.3812-3C>T	XP_011534908.1:n.3812-3C>T
XM_011536607.1:c.2996-3C>T	XP_011534909.1:n.2996-3C>T
XM_011536608.1:c.2903-3C>T	XP_011534910.1:n.2903-3C>T
XM_017021124.1:c.5339-3C>T	XP_016876613.1:n.5339-3C>T
XM_017021125.1:c.5339-3C>T	XP_016876614.1:n.5339-3C>T
XM_017021126.1:c.3830-3C>T	XP_016876615.1:n.3830-3C>T
XM_017021127.2:c.3014-3C>T	XP_016876616.1:n.3014-3C>T
XM_017021128.1:c.2921-3C>T	XP_016876617.1:n.2921-3C>T