Canonical Allele Identifier: CA2144014401

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67752520G= , CM000676.2:g.67752520G=	GRCh38
NC_000014.8:g.68219237G= , CM000676.1:g.68219237G=	GRCh37
NC_000014.7:g.67288990G=	NCBI36
NG_011836.1:g.69070C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.7195C= MANE Select	NP_056161.2:p.Gln2399=
ENST00000347230.9:c.7195C= MANE Select	ENSP00000251119.5:p.Gln2399=
NM_015346.3:c.7195C=	NP_056161.2:p.Gln2399=
ENST00000347230.8:c.7195C=	ENSP00000251119.5:p.Gln2399=
ENST00000394455.6:n.2458C=
ENST00000554523.5:n.7950C=
ENST00000554557.5:c.*5173C=	ENSP00000450431.1:n.*5173C=
ENST00000557306.1:c.733C=	ENSP00000452142.1:p.Gln245=
ENST00000676512.1:c.7213C=	ENSP00000504552.1:p.Gln2405=
ENST00000676620.1:c.7117C=	ENSP00000504587.1:p.Gln2373=
ENST00000678386.1:c.7240C=	ENSP00000503677.1:p.Gln2414=
XM_006720093.2:c.7195C=	XP_006720156.1:p.Gln2399=
XM_011536606.1:c.5686C=	XP_011534908.1:p.Gln1896=
XM_011536607.1:c.4870C=	XP_011534909.1:p.Gln1624=
XM_011536608.1:c.4777C=	XP_011534910.1:p.Gln1593=
XM_017021124.1:c.7213C=	XP_016876613.1:p.Gln2405=
XM_017021125.1:c.7213C=	XP_016876614.1:p.Gln2405=
XM_017021126.1:c.5704C=	XP_016876615.1:p.Gln1902=
XM_017021127.2:c.4888C=	XP_016876616.1:p.Gln1630=
XM_017021128.1:c.4795C=	XP_016876617.1:p.Gln1599=