Canonical Allele Identifier: CA2055548954
Gene: CRADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93850238G= , CM000674.2:g.93850238G= GRCh38
NC_000012.11:g.94244014G= , CM000674.1:g.94244014G= GRCh37
NC_000012.10:g.92768145G= NCBI36
NG_032159.1:g.177864G=
NG_032159.2:g.177864G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332896.8:c.567G= MANE Select ENSP00000327647.3:p.Val189=
ENST00000332896.7:c.567G= ENSP00000327647.3:p.Val189=
ENST00000542893.2:c.567G= ENSP00000439068.2:p.Val189=
ENST00000548330.1:n.952G=
ENST00000548483.5:c.299-43812G= ENSP00000448685.1:n.299-43812G=
ENST00000550030.1:n.367G=
ENST00000551065.5:c.299-9081G= ENSP00000448425.1:n.299-9081G=
ENST00000609189.1:n.343G=
NM_003805.3:c.567G= NP_003796.1:p.Val189=
XM_005269211.3:c.299-43812G= XP_005269268.1:n.299-43812G=
NM_001320099.1:c.567G= NP_001307028.1:p.Val189=
NM_001320100.1:c.299-43812G= NP_001307029.1:n.299-43812G=
NM_003805.4:c.567G= NP_003796.1:p.Val189=
NR_135147.1:n.407-9081G=
XM_017020144.1:c.299-9081G= XP_016875633.1:n.299-9081G=
XR_001748910.1:n.430-9081G=
NM_003805.5:c.567G= MANE Select NP_003796.1:p.Val189=
NM_001320099.2:c.567G= NP_001307028.1:p.Val189=
NM_001320100.2:c.299-43812G= NP_001307029.1:n.299-43812G=
NR_135147.2:n.403-9081G=