Canonical Allele Identifier: CA2144027667

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67782887A= , CM000676.2:g.67782887A=	GRCh38
NC_000014.8:g.68249604A= , CM000676.1:g.68249604A=	GRCh37
NC_000014.7:g.67319357A=	NCBI36
NG_011836.1:g.38703T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4265T= MANE Select	ENSP00000251119.5:p.Val1422=
ENST00000676512.1:c.4265T=	ENSP00000504552.1:p.Val1422=
ENST00000676620.1:c.4265T=	ENSP00000504587.1:p.Val1422=
ENST00000678386.1:c.4265T=	ENSP00000503677.1:p.Val1422=
ENST00000347230.8:c.4265T=	ENSP00000251119.5:p.Val1422=
ENST00000554523.5:n.4402T=
ENST00000554557.5:c.*2350+212T=	ENSP00000450431.1:n.*2350+212T=
ENST00000555452.1:c.4265T=	ENSP00000450603.1:p.Val1422=
NM_015346.3:c.4265T=	NP_056161.2:p.Val1422=
XM_006720093.2:c.4265T=	XP_006720156.1:p.Val1422=
XM_011536606.1:c.2756T=	XP_011534908.1:p.Val919=
XM_011536607.1:c.1940T=	XP_011534909.1:p.Val647=
XM_011536608.1:c.1847T=	XP_011534910.1:p.Val616=
XM_011536609.1:c.4265T=	XP_011534911.1:p.Val1422=
XM_011536609.2:c.4265T=	XP_011534911.1:p.Val1422=
XM_017021124.1:c.4265T=	XP_016876613.1:p.Val1422=
XM_017021125.1:c.4265T=	XP_016876614.1:p.Val1422=
XM_017021126.1:c.2756T=	XP_016876615.1:p.Val919=
XM_017021127.2:c.1940T=	XP_016876616.1:p.Val647=
XM_017021128.1:c.1847T=	XP_016876617.1:p.Val616=
NM_015346.4:c.4265T= MANE Select	NP_056161.2:p.Val1422=