Canonical Allele Identifier: CA796496133

Gene: CRACD

Linked Data

• dbSNP Id: rs1174868450
• gnomAD v3: 4-56276870-A-ACAT
• gnomAD v4: 4-56276870-A-ACAT
• MyVariant Identifiers: chr4:g.57143036_57143037insCAT (hg19) ; chr4:g.56276870_56276871insCAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56276874_56276876dup , CM000666.2:g.56276874_56276876dup	GRCh38
NC_000004.11:g.57143040_57143042dup , CM000666.1:g.57143040_57143042dup	GRCh37
NC_000004.10:g.56837797_56837799dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646253.2:c.239+4382_239+4384dup	ENSP00000495373.2:n.239+4382_239+4384dup
ENST00000629263.3:c.-174+4382_-174+4384dup	ENSP00000486652.1:n.-174+4382_-174+4384dup
ENST00000682029.1:c.-17+4382_-17+4384dup MANE Select	ENSP00000507165.1:n.-17+4382_-17+4384dup
ENST00000264229.11:c.-17+4382_-17+4384dup	ENSP00000264229.6:n.-17+4382_-17+4384dup
ENST00000504228.6:c.-17+4382_-17+4384dup	ENSP00000423366.1:n.-17+4382_-17+4384dup
ENST00000636006.1:c.-17+4382_-17+4384dup	ENSP00000490902.1:n.-17+4382_-17+4384dup
ENST00000646253.1:c.239+4382_239+4384dup	ENSP00000495373.1:n.239+4382_239+4384dup
ENST00000264229.10:c.-17+4382_-17+4384dup	ENSP00000264229.6:n.-17+4382_-17+4384dup
ENST00000503618.1:n.382+4382_382+4384dup
ENST00000504228.5:c.-17+4382_-17+4384dup	ENSP00000423366.1:n.-17+4382_-17+4384dup
ENST00000541073.5:c.-60+4382_-60+4384dup	ENSP00000444006.1:n.-60+4382_-60+4384dup
ENST00000629263.2:c.-174+4382_-174+4384dup	ENSP00000486652.1:n.-174+4382_-174+4384dup
NM_020722.1:c.-17+4382_-17+4384dup	NP_065773.1:n.-17+4382_-17+4384dup
XM_005265752.2:c.-17+4382_-17+4384dup	XP_005265809.1:n.-17+4382_-17+4384dup
XM_011534397.1:c.-17+4382_-17+4384dup	XP_011532699.1:n.-17+4382_-17+4384dup
XM_011534398.1:c.-39+4382_-39+4384dup	XP_011532700.1:n.-39+4382_-39+4384dup
XM_011534399.1:c.-55+4382_-55+4384dup	XP_011532701.1:n.-55+4382_-55+4384dup
XM_011534397.3:c.-17+4382_-17+4384dup	XP_011532699.1:n.-17+4382_-17+4384dup
XM_017008473.1:c.-39+4382_-39+4384dup	XP_016863962.1:n.-39+4382_-39+4384dup
XM_017008474.1:c.-55+4382_-55+4384dup	XP_016863963.1:n.-55+4382_-55+4384dup
XM_024454158.1:c.-17+4382_-17+4384dup	XP_024309926.1:n.-17+4382_-17+4384dup
XM_024454159.1:c.-17+4382_-17+4384dup	XP_024309927.1:n.-17+4382_-17+4384dup
NM_001393381.1:c.-17+4382_-17+4384dup MANE Select	NP_001380310.1:n.-17+4382_-17+4384dup
NM_001393382.1:c.-17+4382_-17+4384dup	NP_001380311.1:n.-17+4382_-17+4384dup
NM_001393383.1:c.-55+4382_-55+4384dup	NP_001380312.1:n.-55+4382_-55+4384dup
NM_001393384.1:c.-55+4382_-55+4384dup	NP_001380313.1:n.-55+4382_-55+4384dup
NM_001393385.1:c.-55+4382_-55+4384dup	NP_001380314.1:n.-55+4382_-55+4384dup
NM_020722.2:c.-17+4382_-17+4384dup	NP_065773.1:n.-17+4382_-17+4384dup