Canonical Allele Identifier: CA2055548570

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850023C= , CM000674.2:g.93850023C=	GRCh38
NC_000012.11:g.94243799C= , CM000674.1:g.94243799C=	GRCh37
NC_000012.10:g.92767930C=	NCBI36
NG_032159.1:g.177649C=
NG_032159.2:g.177649C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.352C= MANE Select	ENSP00000327647.3:p.Arg118=
ENST00000332896.7:c.352C=	ENSP00000327647.3:p.Arg118=
ENST00000542893.2:c.352C=	ENSP00000439068.2:p.Arg118=
ENST00000548330.1:n.737C=
ENST00000548483.5:c.299-44027C=	ENSP00000448685.1:n.299-44027C=
ENST00000550030.1:n.152C=
ENST00000551065.5:c.299-9296C=	ENSP00000448425.1:n.299-9296C=
ENST00000609189.1:n.128C=
NM_003805.3:c.352C=	NP_003796.1:p.Arg118=
XM_005269211.3:c.299-44027C=	XP_005269268.1:n.299-44027C=
NM_001320099.1:c.352C=	NP_001307028.1:p.Arg118=
NM_001320100.1:c.299-44027C=	NP_001307029.1:n.299-44027C=
NM_003805.4:c.352C=	NP_003796.1:p.Arg118=
NR_135147.1:n.407-9296C=
XM_017020144.1:c.299-9296C=	XP_016875633.1:n.299-9296C=
XR_001748908.1:n.657C=
XR_001748910.1:n.430-9296C=
NM_003805.5:c.352C= MANE Select	NP_003796.1:p.Arg118=
NM_001320099.2:c.352C=	NP_001307028.1:p.Arg118=
NM_001320100.2:c.299-44027C=	NP_001307029.1:n.299-44027C=
NR_135147.2:n.403-9296C=