Canonical Allele Identifier: CA2055548626
Gene: CRADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93850062T= , CM000674.2:g.93850062T= GRCh38
NC_000012.11:g.94243838T= , CM000674.1:g.94243838T= GRCh37
NC_000012.10:g.92767969T= NCBI36
NG_032159.1:g.177688T=
NG_032159.2:g.177688T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332896.8:c.391T= MANE Select ENSP00000327647.3:p.Trp131=
ENST00000332896.7:c.391T= ENSP00000327647.3:p.Trp131=
ENST00000542893.2:c.391T= ENSP00000439068.2:p.Trp131=
ENST00000548330.1:n.776T=
ENST00000548483.5:c.299-43988T= ENSP00000448685.1:n.299-43988T=
ENST00000550030.1:n.191T=
ENST00000551065.5:c.299-9257T= ENSP00000448425.1:n.299-9257T=
ENST00000609189.1:n.167T=
NM_003805.3:c.391T= NP_003796.1:p.Trp131=
XM_005269211.3:c.299-43988T= XP_005269268.1:n.299-43988T=
NM_001320099.1:c.391T= NP_001307028.1:p.Trp131=
NM_001320100.1:c.299-43988T= NP_001307029.1:n.299-43988T=
NM_003805.4:c.391T= NP_003796.1:p.Trp131=
NR_135147.1:n.407-9257T=
XM_017020144.1:c.299-9257T= XP_016875633.1:n.299-9257T=
XR_001748910.1:n.430-9257T=
NM_003805.5:c.391T= MANE Select NP_003796.1:p.Trp131=
NM_001320099.2:c.391T= NP_001307028.1:p.Trp131=
NM_001320100.2:c.299-43988T= NP_001307029.1:n.299-43988T=
NR_135147.2:n.403-9257T=