Canonical Allele Identifier: CA262848154

Gene: ZFYVE26

Linked Data

• dbSNP Id: rs886134814
• gnomAD v3: 14-67782632-C-G
• gnomAD v4: 14-67782632-C-G
• MyVariant Identifiers: chr14:g.68249349C>G (hg19) ; chr14:g.67782632C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67782632C>G , CM000676.2:g.67782632C>G	GRCh38
NC_000014.8:g.68249349C>G , CM000676.1:g.68249349C>G	GRCh37
NC_000014.7:g.67319102C>G	NCBI36
NG_011836.1:g.38958G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4372+148G>C MANE Select	ENSP00000251119.5:n.4372+148G>C
ENST00000676512.1:c.4372+148G>C	ENSP00000504552.1:n.4372+148G>C
ENST00000676620.1:c.4372+148G>C	ENSP00000504587.1:n.4372+148G>C
ENST00000678386.1:c.4372+148G>C	ENSP00000503677.1:n.4372+148G>C
ENST00000347230.8:c.4372+148G>C	ENSP00000251119.5:n.4372+148G>C
ENST00000554523.5:n.4509+148G>C
ENST00000554557.5:c.*2350+467G>C	ENSP00000450431.1:n.*2350+467G>C
ENST00000555452.1:c.4372+148G>C	ENSP00000450603.1:n.4372+148G>C
NM_015346.3:c.4372+148G>C	NP_056161.2:n.4372+148G>C
XM_006720093.2:c.4372+148G>C	XP_006720156.1:n.4372+148G>C
XM_011536606.1:c.2863+148G>C	XP_011534908.1:n.2863+148G>C
XM_011536607.1:c.2047+148G>C	XP_011534909.1:n.2047+148G>C
XM_011536608.1:c.1954+148G>C	XP_011534910.1:n.1954+148G>C
XM_011536609.1:c.4372+148G>C	XP_011534911.1:n.4372+148G>C
XM_011536609.2:c.4372+148G>C	XP_011534911.1:n.4372+148G>C
XM_017021124.1:c.4372+148G>C	XP_016876613.1:n.4372+148G>C
XM_017021125.1:c.4372+148G>C	XP_016876614.1:n.4372+148G>C
XM_017021126.1:c.2863+148G>C	XP_016876615.1:n.2863+148G>C
XM_017021127.2:c.2047+148G>C	XP_016876616.1:n.2047+148G>C
XM_017021128.1:c.1954+148G>C	XP_016876617.1:n.1954+148G>C
NM_015346.4:c.4372+148G>C MANE Select	NP_056161.2:n.4372+148G>C