Canonical Allele Identifier: CA2617469168
Gene: CLEC4A HGNC NCBI
ZNF705A HGNC NCBI

Linked Data

gnomAD v4: 12-8138515-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138515T>G , CM000674.2:g.8138515T>G GRCh38
NC_000012.11:g.8291111T>G , CM000674.1:g.8291111T>G GRCh37
NC_000012.10:g.8182378T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229332.12:c.*228T>G (CLEC4A) MANE Select ENSP00000229332.5:n.*228T>G
ENST00000345999.9:c.*228T>G (CLEC4A) ENSP00000344646.3:n.*228T>G
ENST00000402465.8:c.114+262T>G
ENST00000229332.9:c.*228T>G (CLEC4A) ENSP00000229332.5:n.*228T>G
ENST00000345999.7:c.*228T>G (CLEC4A) ENSP00000344646.3:n.*228T>G
ENST00000402465.7:c.-151+262T>G (ZNF705A) ENSP00000384896.3:n.-151+262T>G
NM_016184.3:c.*228T>G (CLEC4A) NP_057268.1:n.*228T>G
NM_194447.2:c.*228T>G (CLEC4A) NP_919429.2:n.*228T>G
NM_194448.2:c.*228T>G (CLEC4A) NP_919430.1:n.*228T>G
NM_194450.2:c.*228T>G (CLEC4A) NP_919432.1:n.*228T>G
XM_011520684.1:c.*228T>G (CLEC4A) XP_011518986.1:n.*228T>G
XM_011520684.2:c.*228T>G (CLEC4A) XP_011518986.1:n.*228T>G
XM_017019382.2:c.*228T>G (CLEC4A) XP_016874871.1:n.*228T>G
XM_024448997.1:c.*228T>G (CLEC4A) XP_024304765.1:n.*228T>G
NM_016184.4:c.*228T>G (CLEC4A) MANE Select NP_057268.1:n.*228T>G
NM_194447.3:c.*228T>G (CLEC4A) NP_919429.2:n.*228T>G
NM_194448.3:c.*228T>G (CLEC4A) NP_919430.1:n.*228T>G
NM_194450.3:c.*228T>G (CLEC4A) NP_919432.1:n.*228T>G