Canonical Allele Identifier: CA1866197513
Gene: ZNF510 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96776788_96776789delinsTC , CM000671.2:g.96776788_96776789delinsTC GRCh38
NC_000009.11:g.99539070_99539071delinsTC , CM000671.1:g.99539070_99539071delinsTC GRCh37
NC_000009.10:g.98578891_98578892delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000223428.9:c.-176-544_-176-543delinsGA MANE Select ENSP00000223428.4:n.-176-544_-176-543delinsGA
ENST00000223428.8:c.-176-544_-176-543delinsGA ENSP00000223428.4:n.-176-544_-176-543delinsGA
ENST00000374641.3:c.-176-544_-176-543delinsGA ENSP00000363772.3:n.-176-544_-176-543delinsGA
ENST00000375231.5:c.-176-544_-176-543delinsGA ENSP00000364379.1:n.-176-544_-176-543delinsGA
NM_001314059.1:c.-176-544_-176-543delinsGA NP_001300988.1:n.-176-544_-176-543delinsGA
NM_001314060.1:c.-303-544_-303-543delinsGA NP_001300989.1:n.-303-544_-303-543delinsGA
NM_014930.1:c.-176-544_-176-543delinsGA NP_055745.1:n.-176-544_-176-543delinsGA
NM_014930.2:c.-176-544_-176-543delinsGA NP_055745.1:n.-176-544_-176-543delinsGA
XM_005251807.2:c.-176-544_-176-543delinsGA XP_005251864.1:n.-176-544_-176-543delinsGA
XM_005251808.2:c.-176-544_-176-543delinsGA XP_005251865.1:n.-176-544_-176-543delinsGA
XM_005251809.2:c.-303-544_-303-543delinsGA XP_005251866.1:n.-303-544_-303-543delinsGA
XM_011518393.2:c.-387-544_-387-543delinsGA XP_011516695.1:n.-387-544_-387-543delinsGA
XM_017014483.1:c.-176-544_-176-543delinsGA XP_016869972.1:n.-176-544_-176-543delinsGA
NM_001314059.2:c.-176-544_-176-543delinsGA NP_001300988.1:n.-176-544_-176-543delinsGA
NM_001314060.2:c.-303-544_-303-543delinsGA NP_001300989.1:n.-303-544_-303-543delinsGA
NM_014930.3:c.-176-544_-176-543delinsGA MANE Select NP_055745.1:n.-176-544_-176-543delinsGA