Canonical Allele Identifier: CA2617469169

Gene: CLEC4A ZNF705A

Linked Data

• gnomAD v4: 12-8138516-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8138516T>G , CM000674.2:g.8138516T>G	GRCh38
NC_000012.11:g.8291112T>G , CM000674.1:g.8291112T>G	GRCh37
NC_000012.10:g.8182379T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000229332.12:c.*229T>G (CLEC4A) MANE Select	ENSP00000229332.5:n.*229T>G
ENST00000345999.9:c.*229T>G (CLEC4A)	ENSP00000344646.3:n.*229T>G
ENST00000402465.8:c.114+263T>G
ENST00000229332.9:c.*229T>G (CLEC4A)	ENSP00000229332.5:n.*229T>G
ENST00000345999.7:c.*229T>G (CLEC4A)	ENSP00000344646.3:n.*229T>G
ENST00000402465.7:c.-151+263T>G (ZNF705A)	ENSP00000384896.3:n.-151+263T>G
NM_016184.3:c.*229T>G (CLEC4A)	NP_057268.1:n.*229T>G
NM_194447.2:c.*229T>G (CLEC4A)	NP_919429.2:n.*229T>G
NM_194448.2:c.*229T>G (CLEC4A)	NP_919430.1:n.*229T>G
NM_194450.2:c.*229T>G (CLEC4A)	NP_919432.1:n.*229T>G
XM_011520684.1:c.*229T>G (CLEC4A)	XP_011518986.1:n.*229T>G
XM_011520684.2:c.*229T>G (CLEC4A)	XP_011518986.1:n.*229T>G
XM_017019382.2:c.*229T>G (CLEC4A)	XP_016874871.1:n.*229T>G
XM_024448997.1:c.*229T>G (CLEC4A)	XP_024304765.1:n.*229T>G
NM_016184.4:c.*229T>G (CLEC4A) MANE Select	NP_057268.1:n.*229T>G
NM_194447.3:c.*229T>G (CLEC4A)	NP_919429.2:n.*229T>G
NM_194448.3:c.*229T>G (CLEC4A)	NP_919430.1:n.*229T>G
NM_194450.3:c.*229T>G (CLEC4A)	NP_919432.1:n.*229T>G