Canonical Allele Identifier: CA2617469185
Gene: CLEC4A HGNC NCBI
ZNF705A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138525_8138526del , CM000674.2:g.8138525_8138526del GRCh38
NC_000012.11:g.8291121_8291122del , CM000674.1:g.8291121_8291122del GRCh37
NC_000012.10:g.8182388_8182389del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229332.12:c.*238_*239del (CLEC4A) MANE Select ENSP00000229332.5:n.*238_*239del
ENST00000345999.9:c.*238_*239del (CLEC4A) ENSP00000344646.3:n.*238_*239del
ENST00000402465.8:c.114+272_114+273del
ENST00000229332.9:c.*238_*239del (CLEC4A) ENSP00000229332.5:n.*238_*239del
ENST00000345999.7:c.*238_*239del (CLEC4A) ENSP00000344646.3:n.*238_*239del
ENST00000402465.7:c.-151+272_-151+273del (ZNF705A) ENSP00000384896.3:n.-151+272_-151+273del
NM_016184.3:c.*238_*239del (CLEC4A) NP_057268.1:n.*238_*239del
NM_194447.2:c.*238_*239del (CLEC4A) NP_919429.2:n.*238_*239del
NM_194448.2:c.*238_*239del (CLEC4A) NP_919430.1:n.*238_*239del
NM_194450.2:c.*238_*239del (CLEC4A) NP_919432.1:n.*238_*239del
XM_011520684.1:c.*238_*239del (CLEC4A) XP_011518986.1:n.*238_*239del
XM_011520684.2:c.*238_*239del (CLEC4A) XP_011518986.1:n.*238_*239del
XM_017019382.2:c.*238_*239del (CLEC4A) XP_016874871.1:n.*238_*239del
XM_024448997.1:c.*238_*239del (CLEC4A) XP_024304765.1:n.*238_*239del
NM_016184.4:c.*238_*239del (CLEC4A) MANE Select NP_057268.1:n.*238_*239del
NM_194447.3:c.*238_*239del (CLEC4A) NP_919429.2:n.*238_*239del
NM_194448.3:c.*238_*239del (CLEC4A) NP_919430.1:n.*238_*239del
NM_194450.3:c.*238_*239del (CLEC4A) NP_919432.1:n.*238_*239del