Canonical Allele Identifier: CA390158431

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67752445G>A , CM000676.2:g.67752445G>A	GRCh38
NC_000014.8:g.68219162G>A , CM000676.1:g.68219162G>A	GRCh37
NC_000014.7:g.67288915G>A	NCBI36
NG_011836.1:g.69145C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.7270C>T MANE Select	NP_056161.2:p.Gln2424Ter
ENST00000347230.9:c.7270C>T MANE Select	ENSP00000251119.5:p.Gln2424Ter
NM_015346.3:c.7270C>T	NP_056161.2:p.Gln2424Ter
ENST00000347230.8:c.7270C>T	ENSP00000251119.5:p.Gln2424Ter
ENST00000394455.6:n.2533C>T
ENST00000554523.5:n.8025C>T
ENST00000554557.5:c.*5248C>T	ENSP00000450431.1:n.*5248C>T
ENST00000557306.1:c.808C>T	ENSP00000452142.1:p.Gln270Ter
ENST00000676512.1:c.7288C>T	ENSP00000504552.1:p.Gln2430Ter
ENST00000676620.1:c.7192C>T	ENSP00000504587.1:p.Gln2398Ter
ENST00000678386.1:c.7315C>T	ENSP00000503677.1:p.Gln2439Ter
XM_006720093.2:c.7270C>T	XP_006720156.1:p.Gln2424Ter
XM_011536606.1:c.5761C>T	XP_011534908.1:p.Gln1921Ter
XM_011536607.1:c.4945C>T	XP_011534909.1:p.Gln1649Ter
XM_011536608.1:c.4852C>T	XP_011534910.1:p.Gln1618Ter
XM_017021124.1:c.7288C>T	XP_016876613.1:p.Gln2430Ter
XM_017021125.1:c.7288C>T	XP_016876614.1:p.Gln2430Ter
XM_017021126.1:c.5779C>T	XP_016876615.1:p.Gln1927Ter
XM_017021127.2:c.4963C>T	XP_016876616.1:p.Gln1655Ter
XM_017021128.1:c.4870C>T	XP_016876617.1:p.Gln1624Ter