Canonical Allele Identifier: CA7238965

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67751055G>A , CM000676.2:g.67751055G>A	GRCh38
NC_000014.8:g.68217772G>A , CM000676.1:g.68217772G>A	GRCh37
NC_000014.7:g.67287525G>A	NCBI36
NG_011836.1:g.70535C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.7413C>T MANE Select	NP_056161.2:p.Asn2471=
ENST00000347230.9:c.7413C>T MANE Select	ENSP00000251119.5:p.Asn2471=
NM_015346.3:c.7413C>T	NP_056161.2:p.Asn2471=
ENST00000347230.8:c.7413C>T	ENSP00000251119.5:p.Asn2471=
ENST00000394455.6:n.2676C>T
ENST00000554523.5:n.8168C>T
ENST00000554557.5:c.*5391C>T	ENSP00000450431.1:n.*5391C>T
ENST00000557306.1:c.951C>T	ENSP00000452142.1:p.Asn317=
ENST00000676512.1:c.7431C>T	ENSP00000504552.1:p.Asn2477=
ENST00000676620.1:c.7335C>T	ENSP00000504587.1:p.Asn2445=
ENST00000678386.1:c.7458C>T	ENSP00000503677.1:p.Asn2486=
XM_006720093.2:c.7413C>T	XP_006720156.1:p.Asn2471=
XM_011536606.1:c.5904C>T	XP_011534908.1:p.Asn1968=
XM_011536607.1:c.5088C>T	XP_011534909.1:p.Asn1696=
XM_011536608.1:c.4995C>T	XP_011534910.1:p.Asn1665=
XM_017021124.1:c.7431C>T	XP_016876613.1:p.Asn2477=
XM_017021125.1:c.7431C>T	XP_016876614.1:p.Asn2477=
XM_017021126.1:c.5922C>T	XP_016876615.1:p.Asn1974=
XM_017021127.2:c.5106C>T	XP_016876616.1:p.Asn1702=
XM_017021128.1:c.5013C>T	XP_016876617.1:p.Asn1671=