Canonical Allele Identifier: CA603179473

Gene: CLEC4A ZNF705A

Linked Data

• dbSNP Id: rs1444597893
• gnomAD v2: 12-8291121-A-G
• gnomAD v3: 12-8138525-A-G
• gnomAD v4: 12-8138525-A-G
• MyVariant Identifiers: chr12:g.8291121A>G (hg19) ; chr12:g.8138525A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8138525A>G , CM000674.2:g.8138525A>G	GRCh38
NC_000012.11:g.8291121A>G , CM000674.1:g.8291121A>G	GRCh37
NC_000012.10:g.8182388A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000229332.12:c.*238A>G (CLEC4A) MANE Select	ENSP00000229332.5:n.*238A>G
ENST00000345999.9:c.*238A>G (CLEC4A)	ENSP00000344646.3:n.*238A>G
ENST00000402465.8:c.114+272A>G
ENST00000229332.9:c.*238A>G (CLEC4A)	ENSP00000229332.5:n.*238A>G
ENST00000345999.7:c.*238A>G (CLEC4A)	ENSP00000344646.3:n.*238A>G
ENST00000402465.7:c.-151+272A>G (ZNF705A)	ENSP00000384896.3:n.-151+272A>G
NM_016184.3:c.*238A>G (CLEC4A)	NP_057268.1:n.*238A>G
NM_194447.2:c.*238A>G (CLEC4A)	NP_919429.2:n.*238A>G
NM_194448.2:c.*238A>G (CLEC4A)	NP_919430.1:n.*238A>G
NM_194450.2:c.*238A>G (CLEC4A)	NP_919432.1:n.*238A>G
XM_011520684.1:c.*238A>G (CLEC4A)	XP_011518986.1:n.*238A>G
XM_011520684.2:c.*238A>G (CLEC4A)	XP_011518986.1:n.*238A>G
XM_017019382.2:c.*238A>G (CLEC4A)	XP_016874871.1:n.*238A>G
XM_024448997.1:c.*238A>G (CLEC4A)	XP_024304765.1:n.*238A>G
NM_016184.4:c.*238A>G (CLEC4A) MANE Select	NP_057268.1:n.*238A>G
NM_194447.3:c.*238A>G (CLEC4A)	NP_919429.2:n.*238A>G
NM_194448.3:c.*238A>G (CLEC4A)	NP_919430.1:n.*238A>G
NM_194450.3:c.*238A>G (CLEC4A)	NP_919432.1:n.*238A>G