Canonical Allele Identifier: CA589298359

Gene: ZNF510

Linked Data

• dbSNP Id: rs1285313888
• gnomAD v2: 9-99539088-C-G
• MyVariant Identifiers: chr9:g.99539088C>G (hg19) ; chr9:g.96776806C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96776806C>G , CM000671.2:g.96776806C>G	GRCh38
NC_000009.11:g.99539088C>G , CM000671.1:g.99539088C>G	GRCh37
NC_000009.10:g.98578909C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000223428.9:c.-176-561G>C MANE Select	ENSP00000223428.4:n.-176-561G>C
ENST00000223428.8:c.-176-561G>C	ENSP00000223428.4:n.-176-561G>C
ENST00000374641.3:c.-176-561G>C	ENSP00000363772.3:n.-176-561G>C
ENST00000375231.5:c.-176-561G>C	ENSP00000364379.1:n.-176-561G>C
NM_001314059.1:c.-176-561G>C	NP_001300988.1:n.-176-561G>C
NM_001314060.1:c.-303-561G>C	NP_001300989.1:n.-303-561G>C
NM_014930.1:c.-176-561G>C	NP_055745.1:n.-176-561G>C
NM_014930.2:c.-176-561G>C	NP_055745.1:n.-176-561G>C
XM_005251807.2:c.-176-561G>C	XP_005251864.1:n.-176-561G>C
XM_005251808.2:c.-176-561G>C	XP_005251865.1:n.-176-561G>C
XM_005251809.2:c.-303-561G>C	XP_005251866.1:n.-303-561G>C
XM_011518393.2:c.-387-561G>C	XP_011516695.1:n.-387-561G>C
XM_017014483.1:c.-176-561G>C	XP_016869972.1:n.-176-561G>C
NM_001314059.2:c.-176-561G>C	NP_001300988.1:n.-176-561G>C
NM_001314060.2:c.-303-561G>C	NP_001300989.1:n.-303-561G>C
NM_014930.3:c.-176-561G>C MANE Select	NP_055745.1:n.-176-561G>C