Canonical Allele Identifier: CA1866197874

Gene: ZNF510

Linked Data

• dbSNP Id: rs1849719784

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96777147A>C , CM000671.2:g.96777147A>C	GRCh38
NC_000009.11:g.99539429A>C , CM000671.1:g.99539429A>C	GRCh37
NC_000009.10:g.98579250A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223428.9:c.-177+887T>G MANE Select	ENSP00000223428.4:n.-177+887T>G
ENST00000223428.8:c.-177+887T>G	ENSP00000223428.4:n.-177+887T>G
ENST00000374641.3:c.-177+887T>G	ENSP00000363772.3:n.-177+887T>G
ENST00000375231.5:c.-177+435T>G	ENSP00000364379.1:n.-177+435T>G
NM_001314059.1:c.-177+435T>G	NP_001300988.1:n.-177+435T>G
NM_001314060.1:c.-304+887T>G	NP_001300989.1:n.-304+887T>G
NM_014930.1:c.-177+887T>G	NP_055745.1:n.-177+887T>G
NM_014930.2:c.-177+887T>G	NP_055745.1:n.-177+887T>G
XM_005251807.2:c.-177+435T>G	XP_005251864.1:n.-177+435T>G
XM_005251808.2:c.-177+887T>G	XP_005251865.1:n.-177+887T>G
XM_005251809.2:c.-304+887T>G	XP_005251866.1:n.-304+887T>G
XM_011518393.2:c.-388+887T>G	XP_011516695.1:n.-388+887T>G
XM_017014483.1:c.-177+435T>G	XP_016869972.1:n.-177+435T>G
NM_001314059.2:c.-177+435T>G	NP_001300988.1:n.-177+435T>G
NM_001314060.2:c.-304+887T>G	NP_001300989.1:n.-304+887T>G
NM_014930.3:c.-177+887T>G MANE Select	NP_055745.1:n.-177+887T>G