Canonical Allele Identifier: CA7240302

Gene: ZFYVE26

Linked Data

• ClinVar Variation Id: 313913
• ClinVar RCV Id: RCV000365485 ; RCV001705470 ; RCV002056412
• dbSNP Id: rs191741115
• ExAC: 14:68260877 A / T
• gnomAD v2: 14-68260877-A-T
• gnomAD v3: 14-67794160-A-T
• gnomAD v4: 14-67794160-A-T
• MyVariant Identifiers: chr14:g.68260877A>T (hg19) ; chr14:g.67794160A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67794160A>T , CM000676.2:g.67794160A>T	GRCh38
NC_000014.8:g.68260877A>T , CM000676.1:g.68260877A>T	GRCh37
NC_000014.7:g.67330630A>T	NCBI36
NG_011836.1:g.27430T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.2401+11T>A MANE Select	ENSP00000251119.5:n.2401+11T>A
ENST00000676512.1:c.2401+11T>A	ENSP00000504552.1:n.2401+11T>A
ENST00000676620.1:c.2401+11T>A	ENSP00000504587.1:n.2401+11T>A
ENST00000677026.1:c.2197+11T>A	ENSP00000503710.1:n.2197+11T>A
ENST00000678382.1:c.*1396+11T>A	ENSP00000504130.1:n.*1396+11T>A
ENST00000678386.1:c.2401+11T>A	ENSP00000503677.1:n.2401+11T>A
ENST00000347230.8:c.2401+11T>A	ENSP00000251119.5:n.2401+11T>A
ENST00000554523.5:n.2538+11T>A
ENST00000554557.5:c.*698+11T>A	ENSP00000450431.1:n.*698+11T>A
ENST00000555452.1:c.2401+11T>A	ENSP00000450603.1:n.2401+11T>A
NM_015346.3:c.2401+11T>A	NP_056161.2:n.2401+11T>A
XM_006720093.2:c.2401+11T>A	XP_006720156.1:n.2401+11T>A
XM_011536606.1:c.892+11T>A	XP_011534908.1:n.892+11T>A
XM_011536607.1:c.76+11T>A	XP_011534909.1:n.76+11T>A
XM_011536608.1:c.-18+11T>A	XP_011534910.1:n.-18+11T>A
XM_011536609.1:c.2401+11T>A	XP_011534911.1:n.2401+11T>A
XM_011536609.2:c.2401+11T>A	XP_011534911.1:n.2401+11T>A
XM_017021124.1:c.2401+11T>A	XP_016876613.1:n.2401+11T>A
XM_017021125.1:c.2401+11T>A	XP_016876614.1:n.2401+11T>A
XM_017021126.1:c.892+11T>A	XP_016876615.1:n.892+11T>A
XM_017021127.2:c.76+11T>A	XP_016876616.1:n.76+11T>A
XM_017021128.1:c.-18+11T>A	XP_016876617.1:n.-18+11T>A
NM_015346.4:c.2401+11T>A MANE Select	NP_056161.2:n.2401+11T>A