Canonical Allele Identifier: CA2055549042

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850289G= , CM000674.2:g.93850289G=	GRCh38
NC_000012.11:g.94244065G= , CM000674.1:g.94244065G=	GRCh37
NC_000012.10:g.92768196G=	NCBI36
NG_032159.1:g.177915G=
NG_032159.2:g.177915G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.*18G= MANE Select	ENSP00000327647.3:n.*18G=
ENST00000332896.7:c.*18G=	ENSP00000327647.3:n.*18G=
ENST00000542893.2:c.*18G=	ENSP00000439068.2:n.*18G=
ENST00000548330.1:n.1003G=
ENST00000548483.5:c.299-43761G=	ENSP00000448685.1:n.299-43761G=
ENST00000550030.1:n.418G=
ENST00000551065.5:c.299-9030G=	ENSP00000448425.1:n.299-9030G=
ENST00000609189.1:n.394G=
NM_003805.3:c.*18G=	NP_003796.1:n.*18G=
XM_005269211.3:c.299-43761G=	XP_005269268.1:n.299-43761G=
NM_001320099.1:c.*18G=	NP_001307028.1:n.*18G=
NM_001320100.1:c.299-43761G=	NP_001307029.1:n.299-43761G=
NM_003805.4:c.*18G=	NP_003796.1:n.*18G=
NR_135147.1:n.407-9030G=
XM_017020144.1:c.299-9030G=	XP_016875633.1:n.299-9030G=
XR_001748910.1:n.430-9030G=
NM_003805.5:c.*18G= MANE Select	NP_003796.1:n.*18G=
NM_001320099.2:c.*18G=	NP_001307028.1:n.*18G=
NM_001320100.2:c.299-43761G=	NP_001307029.1:n.299-43761G=
NR_135147.2:n.403-9030G=