Canonical Allele Identifier: CA2055548461

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93849960_93849961delinsTC , CM000674.2:g.93849960_93849961delinsTC	GRCh38
NC_000012.11:g.94243736_94243737delinsTC , CM000674.1:g.94243736_94243737delinsTC	GRCh37
NC_000012.10:g.92767867_92767868delinsTC	NCBI36
NG_032159.1:g.177586_177587delinsTC
NG_032159.2:g.177586_177587delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.299-10_299-9delinsTC MANE Select	ENSP00000327647.3:n.299-10_299-9delinsTC
ENST00000332896.7:c.299-10_299-9delinsTC	ENSP00000327647.3:n.299-10_299-9delinsTC
ENST00000542893.2:c.299-10_299-9delinsTC	ENSP00000439068.2:n.299-10_299-9delinsTC
ENST00000548330.1:n.684-10_684-9delinsTC
ENST00000548483.5:c.299-44090_299-44089delinsTC	ENSP00000448685.1:n.299-44090_299-44089delinsTC
ENST00000550030.1:n.99-10_99-9delinsTC
ENST00000551065.5:c.299-9359_299-9358delinsTC	ENSP00000448425.1:n.299-9359_299-9358delinsTC
ENST00000609189.1:n.75-10_75-9delinsTC
NM_003805.3:c.299-10_299-9delinsTC	NP_003796.1:n.299-10_299-9delinsTC
XM_005269211.3:c.299-44090_299-44089delinsTC	XP_005269268.1:n.299-44090_299-44089delinsTC
NM_001320099.1:c.299-10_299-9delinsTC	NP_001307028.1:n.299-10_299-9delinsTC
NM_001320100.1:c.299-44090_299-44089delinsTC	NP_001307029.1:n.299-44090_299-44089delinsTC
NM_003805.4:c.299-10_299-9delinsTC	NP_003796.1:n.299-10_299-9delinsTC
NR_135147.1:n.407-9359_407-9358delinsTC
XM_017020144.1:c.299-9359_299-9358delinsTC	XP_016875633.1:n.299-9359_299-9358delinsTC
XR_001748908.1:n.604-10_604-9delinsTC
XR_001748909.1:n.600-10_600-9delinsTC
XR_001748910.1:n.430-9359_430-9358delinsTC
NM_003805.5:c.299-10_299-9delinsTC MANE Select	NP_003796.1:n.299-10_299-9delinsTC
NM_001320099.2:c.299-10_299-9delinsTC	NP_001307028.1:n.299-10_299-9delinsTC
NM_001320100.2:c.299-44090_299-44089delinsTC	NP_001307029.1:n.299-44090_299-44089delinsTC
NR_135147.2:n.403-9359_403-9358delinsTC