Canonical Allele Identifier: CA7881459
Gene: ZNF500 HGNC NCBI

Linked Data

dbSNP Id: rs767487766
gnomAD v2: 16-4812594-G-A
gnomAD v3: 16-4762593-G-A
gnomAD v4: 16-4762593-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4762593G>A , CM000678.2:g.4762593G>A GRCh38
NC_000016.9:g.4812594G>A , CM000678.1:g.4812594G>A GRCh37
NC_000016.8:g.4752595G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219478.11:c.578C>T MANE Select ENSP00000219478.5:p.Pro193Leu
ENST00000219478.10:c.578C>T ENSP00000219478.5:p.Pro193Leu
ENST00000545009.1:c.578C>T ENSP00000445714.1:p.Pro193Leu
ENST00000589422.1:c.*106C>T ENSP00000466375.1:n.*106C>T
NM_001303450.1:c.578C>T NP_001290379.1:p.Pro193Leu
NM_021646.2:c.578C>T NP_067678.1:p.Pro193Leu
XM_005255243.2:c.227C>T XP_005255300.1:p.Pro76Leu
XM_011522453.1:c.578C>T XP_011520755.1:p.Pro193Leu
XM_011522454.1:c.-47C>T XP_011520756.1:n.-47C>T
NM_021646.3:c.578C>T NP_067678.1:p.Pro193Leu
XM_005255243.4:c.227C>T XP_005255300.1:p.Pro76Leu
XM_011522453.2:c.578C>T XP_011520755.1:p.Pro193Leu
XM_011522454.3:c.-47C>T XP_011520756.1:n.-47C>T
XM_017023121.2:c.-47C>T XP_016878610.1:n.-47C>T
NM_001303450.2:c.578C>T NP_001290379.1:p.Pro193Leu
NM_021646.4:c.578C>T MANE Select NP_067678.1:p.Pro193Leu