Canonical Allele Identifier: CA1127108707
Gene: ZNF510 HGNC NCBI

Linked Data

dbSNP Id: rs1849712447

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96776777_96776778del , CM000671.2:g.96776777_96776778del GRCh38
NC_000009.11:g.99539059_99539060del , CM000671.1:g.99539059_99539060del GRCh37
NC_000009.10:g.98578880_98578881del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000223428.9:c.-176-532_-176-531del MANE Select ENSP00000223428.4:n.-176-532_-176-531del
ENST00000223428.8:c.-176-532_-176-531del ENSP00000223428.4:n.-176-532_-176-531del
ENST00000374641.3:c.-176-532_-176-531del ENSP00000363772.3:n.-176-532_-176-531del
ENST00000375231.5:c.-176-532_-176-531del ENSP00000364379.1:n.-176-532_-176-531del
NM_001314059.1:c.-176-532_-176-531del NP_001300988.1:n.-176-532_-176-531del
NM_001314060.1:c.-303-532_-303-531del NP_001300989.1:n.-303-532_-303-531del
NM_014930.1:c.-176-532_-176-531del NP_055745.1:n.-176-532_-176-531del
NM_014930.2:c.-176-532_-176-531del NP_055745.1:n.-176-532_-176-531del
XM_005251807.2:c.-176-532_-176-531del XP_005251864.1:n.-176-532_-176-531del
XM_005251808.2:c.-176-532_-176-531del XP_005251865.1:n.-176-532_-176-531del
XM_005251809.2:c.-303-532_-303-531del XP_005251866.1:n.-303-532_-303-531del
XM_011518393.2:c.-387-532_-387-531del XP_011516695.1:n.-387-532_-387-531del
XM_017014483.1:c.-176-532_-176-531del XP_016869972.1:n.-176-532_-176-531del
NM_001314059.2:c.-176-532_-176-531del NP_001300988.1:n.-176-532_-176-531del
NM_001314060.2:c.-303-532_-303-531del NP_001300989.1:n.-303-532_-303-531del
NM_014930.3:c.-176-532_-176-531del MANE Select NP_055745.1:n.-176-532_-176-531del