Canonical Allele Identifier: CA2838634465

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850261dup , CM000674.2:g.93850261dup	GRCh38
NC_000012.11:g.94244037dup , CM000674.1:g.94244037dup	GRCh37
NC_000012.10:g.92768168dup	NCBI36
NG_032159.1:g.177887dup
NG_032159.2:g.177887dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.590dup MANE Select	ENSP00000327647.3:p.Met197IlefsTer?
ENST00000332896.7:c.590dup	ENSP00000327647.3:p.Met197IlefsTer?
ENST00000542893.2:c.590dup	ENSP00000439068.2:p.Met197IlefsTer?
ENST00000548330.1:n.975dup
ENST00000548483.5:c.299-43789dup	ENSP00000448685.1:n.299-43789dup
ENST00000550030.1:n.390dup
ENST00000551065.5:c.299-9058dup	ENSP00000448425.1:n.299-9058dup
ENST00000609189.1:n.366dup
NM_003805.3:c.590dup	NP_003796.1:p.Met197IlefsTer?
XM_005269211.3:c.299-43789dup	XP_005269268.1:n.299-43789dup
NM_001320099.1:c.590dup	NP_001307028.1:p.Met197IlefsTer?
NM_001320100.1:c.299-43789dup	NP_001307029.1:n.299-43789dup
NM_003805.4:c.590dup	NP_003796.1:p.Met197IlefsTer?
NR_135147.1:n.407-9058dup
XM_017020144.1:c.299-9058dup	XP_016875633.1:n.299-9058dup
XR_001748910.1:n.430-9058dup
NM_003805.5:c.590dup MANE Select	NP_003796.1:p.Met197IlefsTer?
NM_001320099.2:c.590dup	NP_001307028.1:p.Met197IlefsTer?
NM_001320100.2:c.299-43789dup	NP_001307029.1:n.299-43789dup
NR_135147.2:n.403-9058dup