Canonical Allele Identifier: CA2144015060

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67754158G= , CM000676.2:g.67754158G=	GRCh38
NC_000014.8:g.68220875G= , CM000676.1:g.68220875G=	GRCh37
NC_000014.7:g.67290628G=	NCBI36
NG_011836.1:g.67432C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.7041C= MANE Select	NP_056161.2:p.Cys2347=
ENST00000347230.9:c.7041C= MANE Select	ENSP00000251119.5:p.Cys2347=
NM_015346.3:c.7041C=	NP_056161.2:p.Cys2347=
ENST00000347230.8:c.7041C=	ENSP00000251119.5:p.Cys2347=
ENST00000394455.6:n.2304C=
ENST00000554523.5:n.7796C=
ENST00000554557.5:c.*5019C=	ENSP00000450431.1:n.*5019C=
ENST00000554783.1:n.729C=
ENST00000557306.1:c.579C=	ENSP00000452142.1:p.Cys193=
ENST00000676512.1:c.7059C=	ENSP00000504552.1:p.Cys2353=
ENST00000676620.1:c.6963C=	ENSP00000504587.1:p.Cys2321=
ENST00000678386.1:c.7086C=	ENSP00000503677.1:p.Cys2362=
XM_006720093.2:c.7041C=	XP_006720156.1:p.Cys2347=
XM_011536606.1:c.5532C=	XP_011534908.1:p.Cys1844=
XM_011536607.1:c.4716C=	XP_011534909.1:p.Cys1572=
XM_011536608.1:c.4623C=	XP_011534910.1:p.Cys1541=
XM_017021124.1:c.7059C=	XP_016876613.1:p.Cys2353=
XM_017021125.1:c.7059C=	XP_016876614.1:p.Cys2353=
XM_017021126.1:c.5550C=	XP_016876615.1:p.Cys1850=
XM_017021127.2:c.4734C=	XP_016876616.1:p.Cys1578=
XM_017021128.1:c.4641C=	XP_016876617.1:p.Cys1547=