Canonical Allele Identifier: CA390165712

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67766297G>A , CM000676.2:g.67766297G>A	GRCh38
NC_000014.8:g.68233014G>A , CM000676.1:g.68233014G>A	GRCh37
NC_000014.7:g.67302767G>A	NCBI36
NG_011836.1:g.55293C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.5941C>T MANE Select	NP_056161.2:p.Gln1981Ter
ENST00000347230.9:c.5941C>T MANE Select	ENSP00000251119.5:p.Gln1981Ter
NM_015346.3:c.5941C>T	NP_056161.2:p.Gln1981Ter
ENST00000347230.8:c.5941C>T	ENSP00000251119.5:p.Gln1981Ter
ENST00000394455.6:n.1204C>T
ENST00000554523.5:n.6078C>T
ENST00000554557.5:c.*3919C>T	ENSP00000450431.1:n.*3919C>T
ENST00000555452.1:c.5941C>T	ENSP00000450603.1:p.Gln1981Ter
ENST00000676512.1:c.5959C>T	ENSP00000504552.1:p.Gln1987Ter
ENST00000676620.1:c.5863C>T	ENSP00000504587.1:p.Gln1955Ter
ENST00000678386.1:c.5986C>T	ENSP00000503677.1:p.Gln1996Ter
XM_006720093.2:c.5941C>T	XP_006720156.1:p.Gln1981Ter
XM_011536606.1:c.4432C>T	XP_011534908.1:p.Gln1478Ter
XM_011536607.1:c.3616C>T	XP_011534909.1:p.Gln1206Ter
XM_011536608.1:c.3523C>T	XP_011534910.1:p.Gln1175Ter
XM_017021124.1:c.5959C>T	XP_016876613.1:p.Gln1987Ter
XM_017021125.1:c.5959C>T	XP_016876614.1:p.Gln1987Ter
XM_017021126.1:c.4450C>T	XP_016876615.1:p.Gln1484Ter
XM_017021127.2:c.3634C>T	XP_016876616.1:p.Gln1212Ter
XM_017021128.1:c.3541C>T	XP_016876617.1:p.Gln1181Ter