Canonical Allele Identifier: CA2144034030

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67797750G= , CM000676.2:g.67797750G=	GRCh38
NC_000014.8:g.68264467G= , CM000676.1:g.68264467G=	GRCh37
NC_000014.7:g.67334220G=	NCBI36
NG_011836.1:g.23840C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.2254C= MANE Select	NP_056161.2:p.Gln752=
ENST00000347230.9:c.2254C= MANE Select	ENSP00000251119.5:p.Gln752=
NM_015346.3:c.2254C=	NP_056161.2:p.Gln752=
ENST00000347230.8:c.2254C=	ENSP00000251119.5:p.Gln752=
ENST00000554523.5:n.2391C=
ENST00000554557.5:c.*551C=	ENSP00000450431.1:n.*551C=
ENST00000555452.1:c.2254C=	ENSP00000450603.1:p.Gln752=
ENST00000557366.5:n.2300C=
ENST00000557407.1:n.2389C=
ENST00000676512.1:c.2254C=	ENSP00000504552.1:p.Gln752=
ENST00000676620.1:c.2254C=	ENSP00000504587.1:p.Gln752=
ENST00000677026.1:c.2050C=	ENSP00000503710.1:p.Gln684=
ENST00000678382.1:c.*1249C=	ENSP00000504130.1:n.*1249C=
ENST00000678386.1:c.2254C=	ENSP00000503677.1:p.Gln752=
XM_006720093.2:c.2254C=	XP_006720156.1:p.Gln752=
XM_011536606.1:c.745C=	XP_011534908.1:p.Gln249=
XM_011536609.1:c.2254C=	XP_011534911.1:p.Gln752=
XM_011536609.2:c.2254C=	XP_011534911.1:p.Gln752=
XM_017021124.1:c.2254C=	XP_016876613.1:p.Gln752=
XM_017021125.1:c.2254C=	XP_016876614.1:p.Gln752=
XM_017021126.1:c.745C=	XP_016876615.1:p.Gln249=