Canonical Allele Identifier: CA302834835
Gene: ZNF516 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.76471019T>C , CM000680.2:g.76471019T>C GRCh38
NC_000018.9:g.74182975T>C , CM000680.1:g.74182975T>C GRCh37
NC_000018.8:g.72311963T>C NCBI36
NG_032949.1:g.29172A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000443185.7:c.-271-7878A>G MANE Select ENSP00000394757.2:n.-271-7878A>G
ENST00000443185.6:c.-271-7878A>G ENSP00000394757.2:n.-271-7878A>G
ENST00000532857.1:c.-158+19662A>G ENSP00000446211.1:n.-158+19662A>G
NM_014643.3:c.-271-7878A>G NP_055458.1:n.-271-7878A>G
XM_011526269.1:c.-158+20428A>G XP_011524571.1:n.-158+20428A>G
XM_011526270.1:c.-158+19662A>G XP_011524572.1:n.-158+19662A>G
XM_011526271.1:c.-271-7878A>G XP_011524573.1:n.-271-7878A>G
XM_011526272.1:c.-271-7878A>G XP_011524574.1:n.-271-7878A>G
XM_011526273.1:c.-158+24125A>G XP_011524575.1:n.-158+24125A>G
XM_011526274.1:c.-158+23679A>G XP_011524576.1:n.-158+23679A>G
XM_011526275.1:c.-158+20950A>G XP_011524577.1:n.-158+20950A>G
XM_011526276.1:c.-158+20428A>G XP_011524578.1:n.-158+20428A>G
XM_011526277.1:c.-158+20428A>G XP_011524579.1:n.-158+20428A>G
XR_935268.1:n.99+20428A>G
XM_011526269.2:c.-158+20428A>G XP_011524571.1:n.-158+20428A>G
XM_011526270.3:c.-158+19662A>G XP_011524572.1:n.-158+19662A>G
XM_011526271.3:c.-271-7878A>G XP_011524573.1:n.-271-7878A>G
XM_011526273.3:c.-158+24125A>G XP_011524575.1:n.-158+24125A>G
XM_011526274.3:c.-158+23679A>G XP_011524576.1:n.-158+23679A>G
XM_011526275.2:c.-158+20950A>G XP_011524577.1:n.-158+20950A>G
XM_011526276.2:c.-158+20428A>G XP_011524578.1:n.-158+20428A>G
XM_011526277.2:c.-158+20428A>G XP_011524579.1:n.-158+20428A>G
XM_017026097.2:c.-271-7878A>G XP_016881586.1:n.-271-7878A>G
XR_935268.2:n.99+20428A>G
NM_014643.4:c.-271-7878A>G MANE Select NP_055458.1:n.-271-7878A>G
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