Canonical Allele Identifier: CA1866197855

Gene: ZNF510

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96777132_96777135delinsCAGG , CM000671.2:g.96777132_96777135delinsCAGG	GRCh38
NC_000009.11:g.99539414_99539417delinsCAGG , CM000671.1:g.99539414_99539417delinsCAGG	GRCh37
NC_000009.10:g.98579235_98579238delinsCAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223428.9:c.-176-890_-176-887delinsCCTG MANE Select	ENSP00000223428.4:n.-176-890_-176-887delinsCCTG
ENST00000223428.8:c.-176-890_-176-887delinsCCTG	ENSP00000223428.4:n.-176-890_-176-887delinsCCTG
ENST00000374641.3:c.-176-890_-176-887delinsCCTG	ENSP00000363772.3:n.-176-890_-176-887delinsCCTG
ENST00000375231.5:c.-177+447_-177+450delinsCCTG	ENSP00000364379.1:n.-177+447_-177+450delinsCCTG
NM_001314059.1:c.-177+447_-177+450delinsCCTG	NP_001300988.1:n.-177+447_-177+450delinsCCTG
NM_001314060.1:c.-303-890_-303-887delinsCCTG	NP_001300989.1:n.-303-890_-303-887delinsCCTG
NM_014930.1:c.-176-890_-176-887delinsCCTG	NP_055745.1:n.-176-890_-176-887delinsCCTG
NM_014930.2:c.-176-890_-176-887delinsCCTG	NP_055745.1:n.-176-890_-176-887delinsCCTG
XM_005251807.2:c.-177+447_-177+450delinsCCTG	XP_005251864.1:n.-177+447_-177+450delinsCCTG
XM_005251808.2:c.-176-890_-176-887delinsCCTG	XP_005251865.1:n.-176-890_-176-887delinsCCTG
XM_005251809.2:c.-303-890_-303-887delinsCCTG	XP_005251866.1:n.-303-890_-303-887delinsCCTG
XM_011518393.2:c.-387-890_-387-887delinsCCTG	XP_011516695.1:n.-387-890_-387-887delinsCCTG
XM_017014483.1:c.-177+447_-177+450delinsCCTG	XP_016869972.1:n.-177+447_-177+450delinsCCTG
NM_001314059.2:c.-177+447_-177+450delinsCCTG	NP_001300988.1:n.-177+447_-177+450delinsCCTG
NM_001314060.2:c.-303-890_-303-887delinsCCTG	NP_001300989.1:n.-303-890_-303-887delinsCCTG
NM_014930.3:c.-176-890_-176-887delinsCCTG MANE Select	NP_055745.1:n.-176-890_-176-887delinsCCTG