Canonical Allele Identifier: CA919645179
Gene: ZNF500 HGNC NCBI

Linked Data

dbSNP Id: rs1567537220

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4762963_4762965del , CM000678.2:g.4762963_4762965del GRCh38
NC_000016.9:g.4812964_4812966del , CM000678.1:g.4812964_4812966del GRCh37
NC_000016.8:g.4752965_4752967del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219478.11:c.415-206_415-204del MANE Select ENSP00000219478.5:n.415-206_415-204del
ENST00000219478.10:c.415-206_415-204del ENSP00000219478.5:n.415-206_415-204del
ENST00000545009.1:c.415-206_415-204del ENSP00000445714.1:n.415-206_415-204del
ENST00000589422.1:c.415-249_415-247del ENSP00000466375.1:n.415-249_415-247del
NM_001303450.1:c.415-206_415-204del NP_001290379.1:n.415-206_415-204del
NM_021646.2:c.415-206_415-204del NP_067678.1:n.415-206_415-204del
XM_005255243.2:c.64-206_64-204del XP_005255300.1:n.64-206_64-204del
XM_011522453.1:c.415-206_415-204del XP_011520755.1:n.415-206_415-204del
XM_011522454.1:c.-167-249_-167-247del XP_011520756.1:n.-167-249_-167-247del
NM_021646.3:c.415-206_415-204del NP_067678.1:n.415-206_415-204del
XM_005255243.4:c.64-206_64-204del XP_005255300.1:n.64-206_64-204del
XM_011522453.2:c.415-206_415-204del XP_011520755.1:n.415-206_415-204del
XM_011522454.3:c.-167-249_-167-247del XP_011520756.1:n.-167-249_-167-247del
XM_017023121.2:c.-211+29_-211+31del XP_016878610.1:n.-211+29_-211+31del
NM_001303450.2:c.415-206_415-204del NP_001290379.1:n.415-206_415-204del
NM_021646.4:c.415-206_415-204del MANE Select NP_067678.1:n.415-206_415-204del