Canonical Allele Identifier: CA2144027648

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67782844G= , CM000676.2:g.67782844G=	GRCh38
NC_000014.8:g.68249561G= , CM000676.1:g.68249561G=	GRCh37
NC_000014.7:g.67319314G=	NCBI36
NG_011836.1:g.38746C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000347230.9:c.4308C= MANE Select	ENSP00000251119.5:p.Tyr1436=
ENST00000676512.1:c.4308C=	ENSP00000504552.1:p.Tyr1436=
ENST00000676620.1:c.4308C=	ENSP00000504587.1:p.Tyr1436=
ENST00000678386.1:c.4308C=	ENSP00000503677.1:p.Tyr1436=
ENST00000347230.8:c.4308C=	ENSP00000251119.5:p.Tyr1436=
ENST00000554523.5:n.4445C=
ENST00000554557.5:c.*2350+255C=	ENSP00000450431.1:n.*2350+255C=
ENST00000555452.1:c.4308C=	ENSP00000450603.1:p.Tyr1436=
NM_015346.3:c.4308C=	NP_056161.2:p.Tyr1436=
XM_006720093.2:c.4308C=	XP_006720156.1:p.Tyr1436=
XM_011536606.1:c.2799C=	XP_011534908.1:p.Tyr933=
XM_011536607.1:c.1983C=	XP_011534909.1:p.Tyr661=
XM_011536608.1:c.1890C=	XP_011534910.1:p.Tyr630=
XM_011536609.1:c.4308C=	XP_011534911.1:p.Tyr1436=
XM_011536609.2:c.4308C=	XP_011534911.1:p.Tyr1436=
XM_017021124.1:c.4308C=	XP_016876613.1:p.Tyr1436=
XM_017021125.1:c.4308C=	XP_016876614.1:p.Tyr1436=
XM_017021126.1:c.2799C=	XP_016876615.1:p.Tyr933=
XM_017021127.2:c.1983C=	XP_016876616.1:p.Tyr661=
XM_017021128.1:c.1890C=	XP_016876617.1:p.Tyr630=
NM_015346.4:c.4308C= MANE Select	NP_056161.2:p.Tyr1436=