Canonical Allele Identifier: CA1459463612

Gene: CRACD

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56276841C= , CM000666.2:g.56276841C=	GRCh38
NC_000004.11:g.57143007C= , CM000666.1:g.57143007C=	GRCh37
NC_000004.10:g.56837764C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646253.2:c.239+4349C=	ENSP00000495373.2:n.239+4349C=
ENST00000629263.3:c.-174+4349C=	ENSP00000486652.1:n.-174+4349C=
ENST00000682029.1:c.-17+4349C= MANE Select	ENSP00000507165.1:n.-17+4349C=
ENST00000264229.11:c.-17+4349C=	ENSP00000264229.6:n.-17+4349C=
ENST00000504228.6:c.-17+4349C=	ENSP00000423366.1:n.-17+4349C=
ENST00000636006.1:c.-17+4349C=	ENSP00000490902.1:n.-17+4349C=
ENST00000646253.1:c.239+4349C=	ENSP00000495373.1:n.239+4349C=
ENST00000264229.10:c.-17+4349C=	ENSP00000264229.6:n.-17+4349C=
ENST00000503618.1:n.382+4349C=
ENST00000504228.5:c.-17+4349C=	ENSP00000423366.1:n.-17+4349C=
ENST00000541073.5:c.-60+4349C=	ENSP00000444006.1:n.-60+4349C=
ENST00000629263.2:c.-174+4349C=	ENSP00000486652.1:n.-174+4349C=
NM_020722.1:c.-17+4349C=	NP_065773.1:n.-17+4349C=
XM_005265752.2:c.-17+4349C=	XP_005265809.1:n.-17+4349C=
XM_011534397.1:c.-17+4349C=	XP_011532699.1:n.-17+4349C=
XM_011534398.1:c.-39+4349C=	XP_011532700.1:n.-39+4349C=
XM_011534399.1:c.-55+4349C=	XP_011532701.1:n.-55+4349C=
XM_011534397.3:c.-17+4349C=	XP_011532699.1:n.-17+4349C=
XM_017008473.1:c.-39+4349C=	XP_016863962.1:n.-39+4349C=
XM_017008474.1:c.-55+4349C=	XP_016863963.1:n.-55+4349C=
XM_024454158.1:c.-17+4349C=	XP_024309926.1:n.-17+4349C=
XM_024454159.1:c.-17+4349C=	XP_024309927.1:n.-17+4349C=
NM_001393381.1:c.-17+4349C= MANE Select	NP_001380310.1:n.-17+4349C=
NM_001393382.1:c.-17+4349C=	NP_001380311.1:n.-17+4349C=
NM_001393383.1:c.-55+4349C=	NP_001380312.1:n.-55+4349C=
NM_001393384.1:c.-55+4349C=	NP_001380313.1:n.-55+4349C=
NM_001393385.1:c.-55+4349C=	NP_001380314.1:n.-55+4349C=
NM_020722.2:c.-17+4349C=	NP_065773.1:n.-17+4349C=