Canonical Allele Identifier: CA2617469071

Gene: CLEC4A ZNF705A

Linked Data

• gnomAD v4: 12-8138434-CATTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8138436_8138439del , CM000674.2:g.8138436_8138439del	GRCh38
NC_000012.11:g.8291032_8291035del , CM000674.1:g.8291032_8291035del	GRCh37
NC_000012.10:g.8182299_8182302del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229332.12:c.*149_*152del (CLEC4A) MANE Select	ENSP00000229332.5:n.*149_*152del
ENST00000345999.9:c.*149_*152del (CLEC4A)	ENSP00000344646.3:n.*149_*152del
ENST00000402465.8:c.114+183_114+186del
ENST00000229332.9:c.*149_*152del (CLEC4A)	ENSP00000229332.5:n.*149_*152del
ENST00000345999.7:c.*149_*152del (CLEC4A)	ENSP00000344646.3:n.*149_*152del
ENST00000402465.7:c.-151+183_-151+186del (ZNF705A)	ENSP00000384896.3:n.-151+183_-151+186del
NM_016184.3:c.*149_*152del (CLEC4A)	NP_057268.1:n.*149_*152del
NM_194447.2:c.*149_*152del (CLEC4A)	NP_919429.2:n.*149_*152del
NM_194448.2:c.*149_*152del (CLEC4A)	NP_919430.1:n.*149_*152del
NM_194450.2:c.*149_*152del (CLEC4A)	NP_919432.1:n.*149_*152del
XM_011520684.1:c.*149_*152del (CLEC4A)	XP_011518986.1:n.*149_*152del
XM_011520684.2:c.*149_*152del (CLEC4A)	XP_011518986.1:n.*149_*152del
XM_017019382.2:c.*149_*152del (CLEC4A)	XP_016874871.1:n.*149_*152del
XM_024448997.1:c.*149_*152del (CLEC4A)	XP_024304765.1:n.*149_*152del
NM_016184.4:c.*149_*152del (CLEC4A) MANE Select	NP_057268.1:n.*149_*152del
NM_194447.3:c.*149_*152del (CLEC4A)	NP_919429.2:n.*149_*152del
NM_194448.3:c.*149_*152del (CLEC4A)	NP_919430.1:n.*149_*152del
NM_194450.3:c.*149_*152del (CLEC4A)	NP_919432.1:n.*149_*152del