Canonical Allele Identifier: CA390157975

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67752343C>T , CM000676.2:g.67752343C>T	GRCh38
NC_000014.8:g.68219060C>T , CM000676.1:g.68219060C>T	GRCh37
NC_000014.7:g.67288813C>T	NCBI36
NG_011836.1:g.69247G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.7371+1G>A MANE Select	NP_056161.2:n.7371+1G>A
ENST00000347230.9:c.7371+1G>A MANE Select	ENSP00000251119.5:n.7371+1G>A
NM_015346.3:c.7371+1G>A	NP_056161.2:n.7371+1G>A
ENST00000347230.8:c.7371+1G>A	ENSP00000251119.5:n.7371+1G>A
ENST00000394455.6:n.2634+1G>A
ENST00000554523.5:n.8126+1G>A
ENST00000554557.5:c.*5349+1G>A	ENSP00000450431.1:n.*5349+1G>A
ENST00000557306.1:c.909+1G>A	ENSP00000452142.1:n.909+1G>A
ENST00000676512.1:c.7389+1G>A	ENSP00000504552.1:n.7389+1G>A
ENST00000676620.1:c.7293+1G>A	ENSP00000504587.1:n.7293+1G>A
ENST00000678386.1:c.7416+1G>A	ENSP00000503677.1:n.7416+1G>A
XM_006720093.2:c.7371+1G>A	XP_006720156.1:n.7371+1G>A
XM_011536606.1:c.5862+1G>A	XP_011534908.1:n.5862+1G>A
XM_011536607.1:c.5046+1G>A	XP_011534909.1:n.5046+1G>A
XM_011536608.1:c.4953+1G>A	XP_011534910.1:n.4953+1G>A
XM_017021124.1:c.7389+1G>A	XP_016876613.1:n.7389+1G>A
XM_017021125.1:c.7389+1G>A	XP_016876614.1:n.7389+1G>A
XM_017021126.1:c.5880+1G>A	XP_016876615.1:n.5880+1G>A
XM_017021127.2:c.5064+1G>A	XP_016876616.1:n.5064+1G>A
XM_017021128.1:c.4971+1G>A	XP_016876617.1:n.4971+1G>A