Canonical Allele Identifier: CA232592985

Gene: CLEC4A ZNF705A

Linked Data

• dbSNP Id: rs764077224
• gnomAD v2: 12-8291109-C-T
• gnomAD v3: 12-8138513-C-T
• gnomAD v4: 12-8138513-C-T
• MyVariant Identifiers: chr12:g.8291109C>T (hg19) ; chr12:g.8138513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8138513C>T , CM000674.2:g.8138513C>T	GRCh38
NC_000012.11:g.8291109C>T , CM000674.1:g.8291109C>T	GRCh37
NC_000012.10:g.8182376C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000229332.12:c.*226C>T (CLEC4A) MANE Select	ENSP00000229332.5:n.*226C>T
ENST00000345999.9:c.*226C>T (CLEC4A)	ENSP00000344646.3:n.*226C>T
ENST00000402465.8:c.114+260C>T
ENST00000229332.9:c.*226C>T (CLEC4A)	ENSP00000229332.5:n.*226C>T
ENST00000345999.7:c.*226C>T (CLEC4A)	ENSP00000344646.3:n.*226C>T
ENST00000402465.7:c.-151+260C>T (ZNF705A)	ENSP00000384896.3:n.-151+260C>T
NM_016184.3:c.*226C>T (CLEC4A)	NP_057268.1:n.*226C>T
NM_194447.2:c.*226C>T (CLEC4A)	NP_919429.2:n.*226C>T
NM_194448.2:c.*226C>T (CLEC4A)	NP_919430.1:n.*226C>T
NM_194450.2:c.*226C>T (CLEC4A)	NP_919432.1:n.*226C>T
XM_011520684.1:c.*226C>T (CLEC4A)	XP_011518986.1:n.*226C>T
XM_011520684.2:c.*226C>T (CLEC4A)	XP_011518986.1:n.*226C>T
XM_017019382.2:c.*226C>T (CLEC4A)	XP_016874871.1:n.*226C>T
XM_024448997.1:c.*226C>T (CLEC4A)	XP_024304765.1:n.*226C>T
NM_016184.4:c.*226C>T (CLEC4A) MANE Select	NP_057268.1:n.*226C>T
NM_194447.3:c.*226C>T (CLEC4A)	NP_919429.2:n.*226C>T
NM_194448.3:c.*226C>T (CLEC4A)	NP_919430.1:n.*226C>T
NM_194450.3:c.*226C>T (CLEC4A)	NP_919432.1:n.*226C>T