Canonical Allele Identifier: CA944514442
Gene: CLEC4A HGNC NCBI
ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1948167071
gnomAD v4: 12-8138523-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138523A>G , CM000674.2:g.8138523A>G GRCh38
NC_000012.11:g.8291119A>G , CM000674.1:g.8291119A>G GRCh37
NC_000012.10:g.8182386A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229332.12:c.*236A>G (CLEC4A) MANE Select ENSP00000229332.5:n.*236A>G
ENST00000345999.9:c.*236A>G (CLEC4A) ENSP00000344646.3:n.*236A>G
ENST00000402465.8:c.114+270A>G
ENST00000229332.9:c.*236A>G (CLEC4A) ENSP00000229332.5:n.*236A>G
ENST00000345999.7:c.*236A>G (CLEC4A) ENSP00000344646.3:n.*236A>G
ENST00000402465.7:c.-151+270A>G (ZNF705A) ENSP00000384896.3:n.-151+270A>G
NM_016184.3:c.*236A>G (CLEC4A) NP_057268.1:n.*236A>G
NM_194447.2:c.*236A>G (CLEC4A) NP_919429.2:n.*236A>G
NM_194448.2:c.*236A>G (CLEC4A) NP_919430.1:n.*236A>G
NM_194450.2:c.*236A>G (CLEC4A) NP_919432.1:n.*236A>G
XM_011520684.1:c.*236A>G (CLEC4A) XP_011518986.1:n.*236A>G
XM_011520684.2:c.*236A>G (CLEC4A) XP_011518986.1:n.*236A>G
XM_017019382.2:c.*236A>G (CLEC4A) XP_016874871.1:n.*236A>G
XM_024448997.1:c.*236A>G (CLEC4A) XP_024304765.1:n.*236A>G
NM_016184.4:c.*236A>G (CLEC4A) MANE Select NP_057268.1:n.*236A>G
NM_194447.3:c.*236A>G (CLEC4A) NP_919429.2:n.*236A>G
NM_194448.3:c.*236A>G (CLEC4A) NP_919430.1:n.*236A>G
NM_194450.3:c.*236A>G (CLEC4A) NP_919432.1:n.*236A>G