Canonical Allele Identifier: CA944514445
Gene: CLEC4A HGNC NCBI
ZNF705A HGNC NCBI

Linked Data

dbSNP Id: rs1133104
gnomAD v3: 12-8138526-T-C
gnomAD v4: 12-8138526-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138526T>C , CM000674.2:g.8138526T>C GRCh38
NC_000012.11:g.8291122T>C , CM000674.1:g.8291122T>C GRCh37
NC_000012.10:g.8182389T>C NCBI36

Transcript Alleles

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