Canonical Allele Identifier: CA14015676
Gene: ZFYVE26 HGNC NCBI

Linked Data

ClinVar Variation Id: 669979
ClinVar RCV Id: RCV000829094
dbSNP Id: rs12891047

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67776358C>A , CM000676.2:g.67776358C>A GRCh38
NC_000014.8:g.68243075C>A , CM000676.1:g.68243075C>A GRCh37
NC_000014.7:g.67312828C>A NCBI36
NG_011836.1:g.45232G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000347230.9:c.4975-252G>T MANE Select ENSP00000251119.5:n.4975-252G>T
ENST00000676512.1:c.4975-252G>T ENSP00000504552.1:n.4975-252G>T
ENST00000676620.1:c.4975-330G>T ENSP00000504587.1:n.4975-330G>T
ENST00000678386.1:c.5020-252G>T ENSP00000503677.1:n.5020-252G>T
ENST00000347230.8:c.4975-252G>T ENSP00000251119.5:n.4975-252G>T
ENST00000554523.5:n.5112-252G>T
ENST00000554557.5:c.*2953-252G>T ENSP00000450431.1:n.*2953-252G>T
ENST00000555452.1:c.4975-252G>T ENSP00000450603.1:n.4975-252G>T
NM_015346.3:c.4975-252G>T NP_056161.2:n.4975-252G>T
XM_006720093.2:c.4975-252G>T XP_006720156.1:n.4975-252G>T
XM_011536606.1:c.3466-252G>T XP_011534908.1:n.3466-252G>T
XM_011536607.1:c.2650-252G>T XP_011534909.1:n.2650-252G>T
XM_011536608.1:c.2557-252G>T XP_011534910.1:n.2557-252G>T
XM_011536609.1:c.4975-235G>T XP_011534911.1:n.4975-235G>T
XM_011536609.2:c.4975-235G>T XP_011534911.1:n.4975-235G>T
XM_017021124.1:c.4975-252G>T XP_016876613.1:n.4975-252G>T
XM_017021125.1:c.4975-252G>T XP_016876614.1:n.4975-252G>T
XM_017021126.1:c.3466-252G>T XP_016876615.1:n.3466-252G>T
XM_017021127.2:c.2650-252G>T XP_016876616.1:n.2650-252G>T
XM_017021128.1:c.2557-252G>T XP_016876617.1:n.2557-252G>T
NM_015346.4:c.4975-252G>T MANE Select NP_056161.2:n.4975-252G>T