Allele Registry

Canonical Allele Identifier: CA10583179

Gene: ZFYVE26 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr14:g.67769731del

GRCh37 chr14:g.68236448del

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000227299

RCV000330118

ClinVar Variation:

241051

dbSNP:

878855013

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67769731del , CM000676.2:g.67769731del	GRCh38
NC_000014.8:g.68236448del , CM000676.1:g.68236448del	GRCh37
NC_000014.7:g.67306201del	NCBI36
NG_011836.1:g.51859del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.5485-1del MANE Select	ENSP00000251119.5:n.5485-1del
ENST00000676512.1:c.5503-1del	ENSP00000504552.1:n.5503-1del
ENST00000676620.1:c.5407-1del	ENSP00000504587.1:n.5407-1del
ENST00000678386.1:c.5530-1del	ENSP00000503677.1:n.5530-1del
ENST00000347230.8:c.5485-1del	ENSP00000251119.5:n.5485-1del
ENST00000394455.6:n.747del
ENST00000554523.5:n.5622-1del
ENST00000554557.5:c.*3463-1del	ENSP00000450431.1:n.*3463-1del
ENST00000555452.1:c.5485-1del	ENSP00000450603.1:n.5485-1del
NM_015346.3:c.5485-1del	NP_056161.2:n.5485-1del
XM_006720093.2:c.5485-1del	XP_006720156.1:n.5485-1del
XM_011536606.1:c.3976-1del	XP_011534908.1:n.3976-1del
XM_011536607.1:c.3160-1del	XP_011534909.1:n.3160-1del
XM_011536608.1:c.3067-1del	XP_011534910.1:n.3067-1del
XM_017021124.1:c.5503-1del	XP_016876613.1:n.5503-1del
XM_017021125.1:c.5503-1del	XP_016876614.1:n.5503-1del
XM_017021126.1:c.3994-1del	XP_016876615.1:n.3994-1del
XM_017021127.2:c.3178-1del	XP_016876616.1:n.3178-1del
XM_017021128.1:c.3085-1del	XP_016876617.1:n.3085-1del
NM_015346.4:c.5485-1del MANE Select	NP_056161.2:n.5485-1del

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