Canonical Allele Identifier: CA868931805

Gene: ZNF510

Linked Data

• dbSNP Id: rs1309528170
• gnomAD v3: 9-96777132-CAGG-C
• gnomAD v4: 9-96777132-CAGG-C
• MyVariant Identifiers: chr9:g.99539415_99539417del (hg19) ; chr9:g.96777133_96777135del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96777136_96777138del , CM000671.2:g.96777136_96777138del	GRCh38
NC_000009.11:g.99539418_99539420del , CM000671.1:g.99539418_99539420del	GRCh37
NC_000009.10:g.98579239_98579241del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223428.9:c.-176-890_-176-888del MANE Select	ENSP00000223428.4:n.-176-890_-176-888del
ENST00000223428.8:c.-176-890_-176-888del	ENSP00000223428.4:n.-176-890_-176-888del
ENST00000374641.3:c.-176-890_-176-888del	ENSP00000363772.3:n.-176-890_-176-888del
ENST00000375231.5:c.-177+447_-177+449del	ENSP00000364379.1:n.-177+447_-177+449del
NM_001314059.1:c.-177+447_-177+449del	NP_001300988.1:n.-177+447_-177+449del
NM_001314060.1:c.-303-890_-303-888del	NP_001300989.1:n.-303-890_-303-888del
NM_014930.1:c.-176-890_-176-888del	NP_055745.1:n.-176-890_-176-888del
NM_014930.2:c.-176-890_-176-888del	NP_055745.1:n.-176-890_-176-888del
XM_005251807.2:c.-177+447_-177+449del	XP_005251864.1:n.-177+447_-177+449del
XM_005251808.2:c.-176-890_-176-888del	XP_005251865.1:n.-176-890_-176-888del
XM_005251809.2:c.-303-890_-303-888del	XP_005251866.1:n.-303-890_-303-888del
XM_011518393.2:c.-387-890_-387-888del	XP_011516695.1:n.-387-890_-387-888del
XM_017014483.1:c.-177+447_-177+449del	XP_016869972.1:n.-177+447_-177+449del
NM_001314059.2:c.-177+447_-177+449del	NP_001300988.1:n.-177+447_-177+449del
NM_001314060.2:c.-303-890_-303-888del	NP_001300989.1:n.-303-890_-303-888del
NM_014930.3:c.-176-890_-176-888del MANE Select	NP_055745.1:n.-176-890_-176-888del