Canonical Allele Identifier: CA868931817

Gene: ZNF510

Linked Data

• dbSNP Id: rs1436910345
• MyVariant Identifiers: chr9:g.99539420_99539421insGAC (hg19) ; chr9:g.96777138_96777139insGAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96777139_96777141dup , CM000671.2:g.96777139_96777141dup	GRCh38
NC_000009.11:g.99539421_99539423dup , CM000671.1:g.99539421_99539423dup	GRCh37
NC_000009.10:g.98579242_98579244dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223428.9:c.-177+893_-176-894dup MANE Select	ENSP00000223428.4:n.-177+893_-176-894dup
ENST00000223428.8:c.-177+893_-176-894dup	ENSP00000223428.4:n.-177+893_-176-894dup
ENST00000374641.3:c.-177+893_-176-894dup	ENSP00000363772.3:n.-177+893_-176-894dup
ENST00000375231.5:c.-177+441_-177+443dup	ENSP00000364379.1:n.-177+441_-177+443dup
NM_001314059.1:c.-177+441_-177+443dup	NP_001300988.1:n.-177+441_-177+443dup
NM_001314060.1:c.-304+893_-303-894dup	NP_001300989.1:n.-304+893_-303-894dup
NM_014930.1:c.-177+893_-176-894dup	NP_055745.1:n.-177+893_-176-894dup
NM_014930.2:c.-177+893_-176-894dup	NP_055745.1:n.-177+893_-176-894dup
XM_005251807.2:c.-177+441_-177+443dup	XP_005251864.1:n.-177+441_-177+443dup
XM_005251808.2:c.-177+893_-176-894dup	XP_005251865.1:n.-177+893_-176-894dup
XM_005251809.2:c.-304+893_-303-894dup	XP_005251866.1:n.-304+893_-303-894dup
XM_011518393.2:c.-388+893_-387-894dup	XP_011516695.1:n.-388+893_-387-894dup
XM_017014483.1:c.-177+441_-177+443dup	XP_016869972.1:n.-177+441_-177+443dup
NM_001314059.2:c.-177+441_-177+443dup	NP_001300988.1:n.-177+441_-177+443dup
NM_001314060.2:c.-304+893_-303-894dup	NP_001300989.1:n.-304+893_-303-894dup
NM_014930.3:c.-177+893_-176-894dup MANE Select	NP_055745.1:n.-177+893_-176-894dup