Canonical Allele Identifier: CA7239796
Gene: ZFYVE26 HGNC NCBI

Linked Data

ClinVar Variation Id: 1099289
ClinVar RCV Id: RCV001421502
dbSNP Id: rs751803624

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67782829G>A , CM000676.2:g.67782829G>A GRCh38
NC_000014.8:g.68249546G>A , CM000676.1:g.68249546G>A GRCh37
NC_000014.7:g.67319299G>A NCBI36
NG_011836.1:g.38761C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000347230.9:c.4323C>T MANE Select ENSP00000251119.5:p.Asp1441=
ENST00000676512.1:c.4323C>T ENSP00000504552.1:p.Asp1441=
ENST00000676620.1:c.4323C>T ENSP00000504587.1:p.Asp1441=
ENST00000678386.1:c.4323C>T ENSP00000503677.1:p.Asp1441=
ENST00000347230.8:c.4323C>T ENSP00000251119.5:p.Asp1441=
ENST00000554523.5:n.4460C>T
ENST00000554557.5:c.*2350+270C>T ENSP00000450431.1:n.*2350+270C>T
ENST00000555452.1:c.4323C>T ENSP00000450603.1:p.Asp1441=
NM_015346.3:c.4323C>T NP_056161.2:p.Asp1441=
XM_006720093.2:c.4323C>T XP_006720156.1:p.Asp1441=
XM_011536606.1:c.2814C>T XP_011534908.1:p.Asp938=
XM_011536607.1:c.1998C>T XP_011534909.1:p.Asp666=
XM_011536608.1:c.1905C>T XP_011534910.1:p.Asp635=
XM_011536609.1:c.4323C>T XP_011534911.1:p.Asp1441=
XM_011536609.2:c.4323C>T XP_011534911.1:p.Asp1441=
XM_017021124.1:c.4323C>T XP_016876613.1:p.Asp1441=
XM_017021125.1:c.4323C>T XP_016876614.1:p.Asp1441=
XM_017021126.1:c.2814C>T XP_016876615.1:p.Asp938=
XM_017021127.2:c.1998C>T XP_016876616.1:p.Asp666=
XM_017021128.1:c.1905C>T XP_016876617.1:p.Asp635=
NM_015346.4:c.4323C>T MANE Select NP_056161.2:p.Asp1441=