Canonical Allele Identifier: CA2617469076
Gene: CLEC4A HGNC NCBI
ZNF705A HGNC NCBI

Linked Data

gnomAD v4: 12-8138440-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8138440C>A , CM000674.2:g.8138440C>A GRCh38
NC_000012.11:g.8291036C>A , CM000674.1:g.8291036C>A GRCh37
NC_000012.10:g.8182303C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229332.12:c.*153C>A (CLEC4A) MANE Select ENSP00000229332.5:n.*153C>A
ENST00000345999.9:c.*153C>A (CLEC4A) ENSP00000344646.3:n.*153C>A
ENST00000402465.8:c.114+187C>A
ENST00000229332.9:c.*153C>A (CLEC4A) ENSP00000229332.5:n.*153C>A
ENST00000345999.7:c.*153C>A (CLEC4A) ENSP00000344646.3:n.*153C>A
ENST00000402465.7:c.-151+187C>A (ZNF705A) ENSP00000384896.3:n.-151+187C>A
NM_016184.3:c.*153C>A (CLEC4A) NP_057268.1:n.*153C>A
NM_194447.2:c.*153C>A (CLEC4A) NP_919429.2:n.*153C>A
NM_194448.2:c.*153C>A (CLEC4A) NP_919430.1:n.*153C>A
NM_194450.2:c.*153C>A (CLEC4A) NP_919432.1:n.*153C>A
XM_011520684.1:c.*153C>A (CLEC4A) XP_011518986.1:n.*153C>A
XM_011520684.2:c.*153C>A (CLEC4A) XP_011518986.1:n.*153C>A
XM_017019382.2:c.*153C>A (CLEC4A) XP_016874871.1:n.*153C>A
XM_024448997.1:c.*153C>A (CLEC4A) XP_024304765.1:n.*153C>A
NM_016184.4:c.*153C>A (CLEC4A) MANE Select NP_057268.1:n.*153C>A
NM_194447.3:c.*153C>A (CLEC4A) NP_919429.2:n.*153C>A
NM_194448.3:c.*153C>A (CLEC4A) NP_919430.1:n.*153C>A
NM_194450.3:c.*153C>A (CLEC4A) NP_919432.1:n.*153C>A