Canonical Allele Identifier: CA2055548500
Gene: CRADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93850012C= , CM000674.2:g.93850012C= GRCh38
NC_000012.11:g.94243788C= , CM000674.1:g.94243788C= GRCh37
NC_000012.10:g.92767919C= NCBI36
NG_032159.1:g.177638C=
NG_032159.2:g.177638C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332896.8:c.341C= MANE Select ENSP00000327647.3:p.Ser114=
ENST00000332896.7:c.341C= ENSP00000327647.3:p.Ser114=
ENST00000542893.2:c.341C= ENSP00000439068.2:p.Ser114=
ENST00000548330.1:n.726C=
ENST00000548483.5:c.299-44038C= ENSP00000448685.1:n.299-44038C=
ENST00000550030.1:n.141C=
ENST00000551065.5:c.299-9307C= ENSP00000448425.1:n.299-9307C=
ENST00000609189.1:n.117C=
NM_003805.3:c.341C= NP_003796.1:p.Ser114=
XM_005269211.3:c.299-44038C= XP_005269268.1:n.299-44038C=
NM_001320099.1:c.341C= NP_001307028.1:p.Ser114=
NM_001320100.1:c.299-44038C= NP_001307029.1:n.299-44038C=
NM_003805.4:c.341C= NP_003796.1:p.Ser114=
NR_135147.1:n.407-9307C=
XM_017020144.1:c.299-9307C= XP_016875633.1:n.299-9307C=
XR_001748908.1:n.646C=
XR_001748910.1:n.430-9307C=
NM_003805.5:c.341C= MANE Select NP_003796.1:p.Ser114=
NM_001320099.2:c.341C= NP_001307028.1:p.Ser114=
NM_001320100.2:c.299-44038C= NP_001307029.1:n.299-44038C=
NR_135147.2:n.403-9307C=