Canonical Allele Identifier: CA2144019896

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67769731C= , CM000676.2:g.67769731C=	GRCh38
NC_000014.8:g.68236448C= , CM000676.1:g.68236448C=	GRCh37
NC_000014.7:g.67306201C=	NCBI36
NG_011836.1:g.51859G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.5485-1G= MANE Select	NP_056161.2:n.5485-1G=
ENST00000347230.9:c.5485-1G= MANE Select	ENSP00000251119.5:n.5485-1G=
NM_015346.3:c.5485-1G=	NP_056161.2:n.5485-1G=
ENST00000347230.8:c.5485-1G=	ENSP00000251119.5:n.5485-1G=
ENST00000394455.6:n.747G=
ENST00000554523.5:n.5622-1G=
ENST00000554557.5:c.*3463-1G=	ENSP00000450431.1:n.*3463-1G=
ENST00000555452.1:c.5485-1G=	ENSP00000450603.1:n.5485-1G=
ENST00000676512.1:c.5503-1G=	ENSP00000504552.1:n.5503-1G=
ENST00000676620.1:c.5407-1G=	ENSP00000504587.1:n.5407-1G=
ENST00000678386.1:c.5530-1G=	ENSP00000503677.1:n.5530-1G=
XM_006720093.2:c.5485-1G=	XP_006720156.1:n.5485-1G=
XM_011536606.1:c.3976-1G=	XP_011534908.1:n.3976-1G=
XM_011536607.1:c.3160-1G=	XP_011534909.1:n.3160-1G=
XM_011536608.1:c.3067-1G=	XP_011534910.1:n.3067-1G=
XM_017021124.1:c.5503-1G=	XP_016876613.1:n.5503-1G=
XM_017021125.1:c.5503-1G=	XP_016876614.1:n.5503-1G=
XM_017021126.1:c.3994-1G=	XP_016876615.1:n.3994-1G=
XM_017021127.2:c.3178-1G=	XP_016876616.1:n.3178-1G=
XM_017021128.1:c.3085-1G=	XP_016876617.1:n.3085-1G=