Canonical Allele Identifier: CA390170194

Gene: ZFYVE26

Linked Data

• ClinVar Variation Id: 2621735
• ClinVar RCV Id: RCV003372384
• MyVariant Identifiers: chr14:g.68249565A>T (hg19) ; chr14:g.67782848A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67782848A>T , CM000676.2:g.67782848A>T	GRCh38
NC_000014.8:g.68249565A>T , CM000676.1:g.68249565A>T	GRCh37
NC_000014.7:g.67319318A>T	NCBI36
NG_011836.1:g.38742T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347230.9:c.4304T>A MANE Select	ENSP00000251119.5:p.Val1435Glu
ENST00000676512.1:c.4304T>A	ENSP00000504552.1:p.Val1435Glu
ENST00000676620.1:c.4304T>A	ENSP00000504587.1:p.Val1435Glu
ENST00000678386.1:c.4304T>A	ENSP00000503677.1:p.Val1435Glu
ENST00000347230.8:c.4304T>A	ENSP00000251119.5:p.Val1435Glu
ENST00000554523.5:n.4441T>A
ENST00000554557.5:c.*2350+251T>A	ENSP00000450431.1:n.*2350+251T>A
ENST00000555452.1:c.4304T>A	ENSP00000450603.1:p.Val1435Glu
NM_015346.3:c.4304T>A	NP_056161.2:p.Val1435Glu
XM_006720093.2:c.4304T>A	XP_006720156.1:p.Val1435Glu
XM_011536606.1:c.2795T>A	XP_011534908.1:p.Val932Glu
XM_011536607.1:c.1979T>A	XP_011534909.1:p.Val660Glu
XM_011536608.1:c.1886T>A	XP_011534910.1:p.Val629Glu
XM_011536609.1:c.4304T>A	XP_011534911.1:p.Val1435Glu
XM_011536609.2:c.4304T>A	XP_011534911.1:p.Val1435Glu
XM_017021124.1:c.4304T>A	XP_016876613.1:p.Val1435Glu
XM_017021125.1:c.4304T>A	XP_016876614.1:p.Val1435Glu
XM_017021126.1:c.2795T>A	XP_016876615.1:p.Val932Glu
XM_017021127.2:c.1979T>A	XP_016876616.1:p.Val660Glu
XM_017021128.1:c.1886T>A	XP_016876617.1:p.Val629Glu
NM_015346.4:c.4304T>A MANE Select	NP_056161.2:p.Val1435Glu