Canonical Allele Identifier: CA14540334

Gene: CD226

Linked Data

• dbSNP Id: rs1788229
• gnomAD v2: 18-67533961-T-G
• gnomAD v3: 18-69866725-T-G
• gnomAD v4: 18-69866725-T-G
• MyVariant Identifiers: chr18:g.67533961T>G (hg19) ; chr18:g.69866725T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.69866725T>G , CM000680.2:g.69866725T>G	GRCh38
NC_000018.9:g.67533961T>G , CM000680.1:g.67533961T>G	GRCh37
NC_000018.8:g.65684941T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000582621.6:c.885+632A>C MANE Select	ENSP00000461947.1:n.885+632A>C
ENST00000280200.8:c.885+632A>C	ENSP00000280200.4:n.885+632A>C
ENST00000577287.5:c.420+632A>C	ENSP00000462453.1:n.420+632A>C
ENST00000578928.1:c.110-24330A>C	ENSP00000463152.1:n.110-24330A>C
ENST00000581982.5:c.420+632A>C	ENSP00000464084.1:n.420+632A>C
ENST00000582621.5:c.885+632A>C	ENSP00000461947.1:n.885+632A>C
NM_001303618.1:c.885+632A>C	NP_001290547.1:n.885+632A>C
NM_001303619.1:c.420+632A>C	NP_001290548.1:n.420+632A>C
NM_006566.3:c.885+632A>C	NP_006557.2:n.885+632A>C
XM_005266642.2:c.885+632A>C	XP_005266699.1:n.885+632A>C
XM_005266643.2:c.420+632A>C	XP_005266700.1:n.420+632A>C
XM_006722374.2:c.516+632A>C	XP_006722437.1:n.516+632A>C
XM_005266642.3:c.885+632A>C	XP_005266699.1:n.885+632A>C
XM_005266643.3:c.420+632A>C	XP_005266700.1:n.420+632A>C
XM_006722374.3:c.516+632A>C	XP_006722437.1:n.516+632A>C
XM_017025525.1:c.420+632A>C	XP_016881014.1:n.420+632A>C
XM_017025526.1:c.420+632A>C	XP_016881015.1:n.420+632A>C
XM_017025527.1:c.420+632A>C	XP_016881016.1:n.420+632A>C
NM_001303618.2:c.885+632A>C MANE Select	NP_001290547.1:n.885+632A>C
NM_001303619.2:c.420+632A>C	NP_001290548.1:n.420+632A>C
NM_006566.4:c.885+632A>C	NP_006557.2:n.885+632A>C