Canonical Allele Identifier: CA356980189

Gene: CRACD

Linked Data

• ClinVar Variation Id: 3077091
• ClinVar RCV Id: RCV004374867
• gnomAD v4: 4-56315214-A-G
• MyVariant Identifiers: chr4:g.57181380A>G (hg19) ; chr4:g.56315214A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56315214A>G , CM000666.2:g.56315214A>G	GRCh38
NC_000004.11:g.57181380A>G , CM000666.1:g.57181380A>G	GRCh37
NC_000004.10:g.56876137A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646253.2:c.1967A>G	ENSP00000495373.2:p.Gln656Arg
ENST00000682029.1:c.1712A>G MANE Select	ENSP00000507165.1:p.Gln571Arg
ENST00000264229.11:c.1712A>G	ENSP00000264229.6:p.Gln571Arg
ENST00000504228.6:c.1712A>G	ENSP00000423366.1:p.Gln571Arg
ENST00000264229.10:c.1712A>G	ENSP00000264229.6:p.Gln571Arg
ENST00000504228.5:c.1712A>G	ENSP00000423366.1:p.Gln571Arg
ENST00000541073.5:c.1691A>G	ENSP00000444006.1:p.Gln564Arg
NM_020722.1:c.1712A>G	NP_065773.1:p.Gln571Arg
XM_005265752.2:c.1712A>G	XP_005265809.1:p.Gln571Arg
XM_005265755.2:c.1466A>G	XP_005265812.1:p.Gln489Arg
XM_005265756.2:c.1442A>G	XP_005265813.1:p.Gln481Arg
XM_006714045.2:c.1370A>G	XP_006714108.1:p.Gln457Arg
XM_011534395.1:c.1808A>G	XP_011532697.1:p.Gln603Arg
XM_011534396.1:c.1790A>G	XP_011532698.1:p.Gln597Arg
XM_011534397.1:c.1712A>G	XP_011532699.1:p.Gln571Arg
XM_011534398.1:c.1712A>G	XP_011532700.1:p.Gln571Arg
XM_011534399.1:c.1538A>G	XP_011532701.1:p.Gln513Arg
XM_011534400.1:c.1538A>G	XP_011532702.1:p.Gln513Arg
XM_011534397.3:c.1712A>G	XP_011532699.1:p.Gln571Arg
XM_017008473.1:c.1712A>G	XP_016863962.1:p.Gln571Arg
XM_017008474.1:c.1538A>G	XP_016863963.1:p.Gln513Arg
XM_024454158.1:c.1712A>G	XP_024309926.1:p.Gln571Arg
XM_024454159.1:c.1712A>G	XP_024309927.1:p.Gln571Arg
NM_001393381.1:c.1712A>G MANE Select	NP_001380310.1:p.Gln571Arg
NM_001393382.1:c.1712A>G	NP_001380311.1:p.Gln571Arg
NM_001393383.1:c.1538A>G	NP_001380312.1:p.Gln513Arg
NM_001393384.1:c.1538A>G	NP_001380313.1:p.Gln513Arg
NM_001393385.1:c.1538A>G	NP_001380314.1:p.Gln513Arg
NM_020722.2:c.1712A>G	NP_065773.1:p.Gln571Arg