Canonical Allele Identifier: CA406527412
Gene: ZNF227 HGNC NCBI
ZNF235 HGNC NCBI

Linked Data

ClinVar Variation Id: 441021
ClinVar RCV Id: RCV000509507
dbSNP Id: rs1555794654

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44236663A>T , CM000681.2:g.44236663A>T GRCh38
NC_000019.9:g.44740816A>T , CM000681.1:g.44740816A>T GRCh37
NC_000019.8:g.49432656A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000313040.12:c.2233A>T (ZNF227) MANE Select ENSP00000321049.6:p.Lys745Ter
ENST00000313040.11:c.2233A>T (ZNF227) ENSP00000321049.6:p.Lys745Ter
ENST00000391961.6:c.2080A>T (ZNF227) ENSP00000375823.2:p.Lys694Ter
ENST00000589005.5:c.2080A>T (ZNF227) ENSP00000467577.1:p.Lys694Ter
ENST00000589799.5:c.*53T>A (ZNF235) ENSP00000468695.1:n.*53T>A
ENST00000592844.5:c.239-1794T>A (ZNF235) ENSP00000465641.1:n.239-1794T>A
ENST00000621083.4:c.2233A>T (ZNF227) ENSP00000482749.1:p.Lys745Ter
NM_001289166.1:c.2233A>T (ZNF227) NP_001276095.1:p.Lys745Ter
NM_001289167.1:c.2080A>T (ZNF227) NP_001276096.1:p.Lys694Ter
NM_001289168.1:c.2080A>T (ZNF227) NP_001276097.1:p.Lys694Ter
NM_001289169.1:c.2080A>T (ZNF227) NP_001276098.1:p.Lys694Ter
NM_001289170.1:c.1996A>T (ZNF227) NP_001276099.1:p.Lys666Ter
NM_001289171.1:c.1996A>T (ZNF227) NP_001276100.1:p.Lys666Ter
NM_001289172.1:c.1942A>T (ZNF227) NP_001276101.1:p.Lys648Ter
NM_001289173.1:c.2149A>T (ZNF227) NP_001276102.1:p.Lys717Ter
NM_182490.2:c.2233A>T (ZNF227) NP_872296.1:p.Lys745Ter
XM_005259232.1:c.2233A>T (ZNF227) XP_005259289.1:p.Lys745Ter
XM_006723371.1:c.2149A>T (ZNF227) XP_006723434.1:p.Lys717Ter
XM_011527289.1:c.2233A>T (ZNF227) XP_011525591.1:p.Lys745Ter
XM_011527290.1:c.2212A>T (ZNF227) XP_011525592.1:p.Lys738Ter
XM_011527291.1:c.2023A>T (ZNF227) XP_011525593.1:p.Lys675Ter
XM_005259232.3:c.2233A>T (ZNF227) XP_005259289.1:p.Lys745Ter
XM_011527289.2:c.2233A>T (ZNF227) XP_011525591.1:p.Lys745Ter
XM_017027266.1:c.2233A>T (ZNF227) XP_016882755.1:p.Lys745Ter
XM_017027267.1:c.2149A>T (ZNF227) XP_016882756.1:p.Lys717Ter
XM_017027268.1:c.2080A>T (ZNF227) XP_016882757.1:p.Lys694Ter
XM_017027269.2:c.2080A>T (ZNF227) XP_016882758.1:p.Lys694Ter
XM_017027270.1:c.2080A>T (ZNF227) XP_016882759.1:p.Lys694Ter
XM_017027271.2:c.2080A>T (ZNF227) XP_016882760.1:p.Lys694Ter
XM_017027272.1:c.2059A>T (ZNF227) XP_016882761.1:p.Lys687Ter
XM_017027273.2:c.2059A>T (ZNF227) XP_016882762.1:p.Lys687Ter
XM_017027274.2:c.2059A>T (ZNF227) XP_016882763.1:p.Lys687Ter
XM_017027275.1:c.2023A>T (ZNF227) XP_016882764.1:p.Lys675Ter
XM_017027276.2:c.2023A>T (ZNF227) XP_016882765.1:p.Lys675Ter
XM_017027277.1:c.2023A>T (ZNF227) XP_016882766.1:p.Lys675Ter
XM_017027278.1:c.2023A>T (ZNF227) XP_016882767.1:p.Lys675Ter
XM_017027279.1:c.1996A>T (ZNF227) XP_016882768.1:p.Lys666Ter
NM_182490.3:c.2233A>T (ZNF227) MANE Select NP_872296.1:p.Lys745Ter
NM_001289166.2:c.2233A>T (ZNF227) NP_001276095.1:p.Lys745Ter
NM_001289167.2:c.2080A>T (ZNF227) NP_001276096.1:p.Lys694Ter
NM_001289168.2:c.2080A>T (ZNF227) NP_001276097.1:p.Lys694Ter
NM_001289169.2:c.2080A>T (ZNF227) NP_001276098.1:p.Lys694Ter
NM_001289170.2:c.1996A>T (ZNF227) NP_001276099.1:p.Lys666Ter
NM_001289171.2:c.1996A>T (ZNF227) NP_001276100.1:p.Lys666Ter
NM_001289172.2:c.1942A>T (ZNF227) NP_001276101.1:p.Lys648Ter
NM_001289173.2:c.2149A>T (ZNF227) NP_001276102.1:p.Lys717Ter